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Bioguard Burn Dressing - Ready-Cut Gauze

FDA UDI

Class II (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
Bioguard Burn Dressing - Ready-Cut Gauze FDA UDI
Generic Name
Synthetic nanofiber barrier dressing FDA UDI
Device Name
Bioguard Burn Dressing - Ready-Cut Gauze, 100 Ply - Mesh Gauze 18 in x 18 in (45.7 cm x 45.7 cm) FDA UDI
Model / Reference
97118 FDA UDI
Description
Bioguard Burn Dressing - Ready-Cut Gauze, 100 Ply - Mesh Gauze 18 in x 18 in (45.7 cm x 45.7 cm) FDA UDI

Identifiers

Catalog Number
97118 FDA UDI
Primary DI / UDI-DI
00809958088906 FDA UDI
FDA Product Code
NYS FDA UDI
GMDN Term
Synthetic nanofiber barrier dressing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4015 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Bioguard Burn Dressing - Ready-Cut Gauze by Derma Sciences Canada, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 958cbabf-f7ee-4359-b0f1-26320565125e 36 fields · synced May 30, 2026