Identity
- Trade Name
- DeRoyal FDA UDI
- Generic Name
- Razor blade FDA UDI
- Device Name
- Custom Razor Blade FDA UDI
- Model / Reference
- 32-1992 FDA UDI
- Description
- Custom Razor Blade FDA UDI
Identifiers
- Catalog Number
- 32-1992 FDA UDI
- Primary DI / UDI-DI
- 00749756817875 FDA UDI
- FDA Product Code
- LWK 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Razor blade
DeRoyal by Deroyal Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Razor blade.
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
- Dermapac, Inc. — Dermapac Inc. · Class I
- NATIONAL HOSPITAL PACKAGING — Surgi-Pak, Inc. · Class I
- GRAFCO — GF Health Products, Inc · Class I
- Dermapac, Inc. — Dermapac Inc. · Class I
- ASP MEDICAL — Asp Global, LLC · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Deroyal Industries, Inc.
Sources (1)
- FDA UDI 5a8b633e-1e9a-4c7c-8c7f-9d9fada938ba 35 fields · synced Jun 8, 2026