Identity
- Trade Name
- Wexler Surgical, Inc. FDA UDI
- Generic Name
- Surgical vessel loop FDA UDI
- Model / Reference
- DL0100-B FDA UDI
Identifiers
- Primary DI / UDI-DI
- M944DL0100B0 FDA UDI
- FDA Product Code
- HCF FDA UDI
- GMDN Term
- Surgical vessel loop 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical vessel loop
Wexler Surgical, Inc. by Wexler Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Devon — Cardinal Health 200, LLC · 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
- Wexler Surgical, Inc.
Sources (1)
- FDA UDI f96774e8-00a0-447b-ad01-7dc70942d01d 32 fields · synced Jun 9, 2026