Identity
- Trade Name
- REMOVER FDA UDI
- Generic Name
- Scalpel blade remover FDA UDI
- Device Name
- SCALPEL BLADE FDA UDI
- Model / Reference
- 10-199-00-01 FDA UDI
- Description
- SCALPEL BLADE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888118011602 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Scalpel blade remover 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Scalpel blade remover
Remover by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Scalpel blade remover.
- BladeFLASK — QLICKSMART PTY LTD · Class II
- Sklar — Sklar Corporation · Class I
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- gSource — GSOURCE, LLC. · Class I
- EZ-Blade Remover — DXM CO., LTD · Class I
- BladeFlask EVO Blade Remover — QLICKSMART PTY LTD · Class I
- Hayden Medical — Hayden Medical 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 |
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Manufacturer
- Manufacturer
- KLS-Martin L.P.
Sources (1)
- FDA UDI c6859ca1-d9b8-4a7b-9cfd-97578b951489 34 fields · synced Jun 1, 2026