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Product Image-118-0057

Refill for first aid panel

Catalog Number: (118-0057)
Supplier: ORKLA CARE
Description: Refill pack for the first aid panel, for use in first aid situations.
UOM: 1 * 1 items
Product Image-BINH1008541

Torso

Supplier: 3B Scientific
Description: This easy to transport torso allows the practice of adult CPR techniques. Optionally child CPR can also be practiced by changing the supplied springs inside the torso. Individual student face masks with a one-way non-rebreathing valve and disposable airways provide maximum protection against cross-contamination.

Product Image-BINH1000194

Mini-Torso, without head, 9-part

Catalog Number: (BINH1000194)
Supplier: 3B Scientific
Description: This human mini torso is approximately half life-size, supplied with the 3B Torso Guide. Even small hands can quickly disassemble and assemble this torso. This torso includes the following parts and organs:
UOM: 1 * 1 items
Image Unavailable-BOSSBS-7593R-CY5.5

Anti-GLA Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-7593R-CY5.5)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-CY7

Anti-GLA Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-7593R-CY7)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Product Image-761-0001

Models of torso

Supplier: 3B Scientific
Description: This school torso is supplied with the following parts: 3-part head, 2 lungs, 2-part heart, stomach, liver with gall bladder, 2-part intestinal tract, front half of kidney, front half of urinary bladder.

Image Unavailable-BOSSBS-7593R-A647

Anti-GLA Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-7593R-A647)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-HRP

Anti-GLA Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-7593R-HRP)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Product Image-118-0247

Eye and wound cleansing spray

Catalog Number: (118-0247)
Supplier: ORKLA CARE
Description: This cleansing spray is intended for rinsing and cleaning out dust and dirt from eyes and wounds. The portable spray bottle is filled with 150 ml physiological (0,9%) unbuffered sodium chloride solution.
UOM: 1 * 1 items
Product Image-118-0025

Wound cleansers

Supplier: ORKLA CARE
Description: Wound cleansers do away with cotton wool and bottles of antiseptic. These sterile, non woven tissues, which are saturated in a wound cleansing fluid (0,9% NaCl), are intended for the mechanical cleansing of minor wounds when clean tap water is not available.

Image Unavailable-BOSSBS-7593R-CY5

Anti-GLA Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-7593R-CY5)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-CY3

Anti-GLA Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-7593R-CY3)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-A555

Anti-GLA Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-7593R-A555)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-A488

Anti-GLA Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-7593R-A488)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-A680

Anti-Galactosidase alpha Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-7593R-A680)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-A750

Anti-Galactosidase alpha Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-7593R-A750)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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