Identity
- Trade Name
- Bioguard Island Dressing FDA UDI
- Generic Name
- Synthetic nanofiber barrier dressing FDA UDI
- Device Name
- Bioguard Island Dressing, 4 in x 10 in (10.2 cm x 25.4 cm) FDA UDI
- Model / Reference
- 97041 FDA UDI
- Description
- Bioguard Island Dressing, 4 in x 10 in (10.2 cm x 25.4 cm) FDA UDI
Identifiers
- Catalog Number
- 97041 FDA UDI
- Primary DI / UDI-DI
- 00809958088401 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 Island Dressing 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 22cab001-a3e6-4192-8f1f-8fb86e236ce3 36 fields · synced May 30, 2026