Identity
- Trade Name
- Dermapac, Inc. FDA UDI
- Generic Name
- Razor blade FDA UDI
- Device Name
- Weck Blades 5/pk FDA UDI
- Model / Reference
- 8807 FDA UDI
- Description
- Weck Blades 5/pk FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10810102271386 FDA UDI
- FDA Product Code
- GES FDA UDI
- GMDN Term
- Razor blade FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Razor blade
Dermapac, Inc. by Dermapac Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Dermapac Inc.
Sources (1)
- FDA UDI aaf4f2c3-d96c-4925-9f4a-e7e7756b8eaa 34 fields · synced May 30, 2026