Identity
- Trade Name
- EZ-Blade Remover FDA UDI
- Generic Name
- Scalpel blade remover FDA UDI
- Device Name
- Disposable Blade Remover is a simple but efficient way to prevent cuts, scrapes, and possible infection when removing and disposing blades with no direct contact with the blade Easily and securely remove used scalpel blades for disposal • Palm-sized round design made with rigid and durable polypropylene • User is able to safely and hygienically remove the blades with one simple pull • Store up to 100 blades • Store not only used scalpel blades but also medical needles, dermaplaning tools, dermaplaning razors, and other small blades FDA UDI
- Model / Reference
- EZ-Blade Remover FDA UDI
- Description
- Disposable Blade Remover is a simple but efficient way to prevent cuts, scrapes, and possible infection when removing and disposing blades with no direct contact with the blade Easily and securely remove used scalpel blades for disposal • Palm-sized round design made with rigid and durable polypropylene • User is able to safely and hygienically remove the blades with one simple pull • Store up to 100 blades • Store not only used scalpel blades but also medical needles, dermaplaning tools, dermaplaning razors, and other small blades FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800017901688 FDA UDI
- FDA Product Code
- GES 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
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Scalpel blade remover
EZ-Blade Remover by Dxm Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Scalpel blade remover.
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- gSource — GSOURCE, LLC. · Class I
- BladeFlask EVO Blade Remover — QLICKSMART PTY LTD · Class I
- Hayden Medical — Hayden Medical Inc · Class I
- BladeFlask EVO — QLICKSMART PTY LTD · Class II
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
- Dxm Co., Ltd
Sources (1)
- FDA UDI c55a0206-d889-4860-a3c6-8855bc9d0694 33 fields · synced Jun 8, 2026