Identity
- Trade Name
- Devon FDA UDI
- Generic Name
- Surgical vessel loop FDA UDI
- Device Name
- Mini Blue Vessel Loops, Bulk Non-Sterile, 1000EA/CS FDA UDI
- Model / Reference
- 28000-01B FDA UDI
- Description
- Mini Blue Vessel Loops, Bulk Non-Sterile, 1000EA/CS FDA UDI
Identifiers
- Catalog Number
- 28000-01B FDA UDI
- Primary DI / UDI-DI
- 50885380180116 FDA UDI
- FDA Product Code
- KDC 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Surgical vessel loop
Devon by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical vessel loop.
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- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class I
- Degania — DEGANIA SILICONE LTD · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Scanlan® SURG-I-LOOP® silicone loops — SCANLAN INTERNATIONAL 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
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 647aaa6c-901f-46ec-a25c-78ede79526eb 34 fields · synced Jun 8, 2026