Identity
- Trade Name
- Bioguard Conforming Bandage FDA UDI
- Generic Name
- Synthetic nanofiber barrier dressing FDA UDI
- Device Name
- Bioguard Conforming Bandage, 2 in x 4.1 yd (5.1 cm x 3.7 cm), Stretched, 1 Roll FDA UDI
- Model / Reference
- 97241 FDA UDI
- Description
- Bioguard Conforming Bandage, 2 in x 4.1 yd (5.1 cm x 3.7 cm), Stretched, 1 Roll FDA UDI
Identifiers
- Catalog Number
- 97241 FDA UDI
- Primary DI / UDI-DI
- 00809958088708 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Bioguard Conforming Bandage 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Derma Sciences Canada, Inc
Sources (1)
- FDA UDI fbaad16f-6f0e-4a2b-9e44-d4531155e5dc 35 fields · synced Jun 1, 2026