Identity
- Trade Name
- HAVEL'S FDA UDI
- Generic Name
- Silk suture FDA UDI
- Device Name
- SUTURE 3-0 SILK 18"/HS-24 FDA UDI
- Model / Reference
- SUT. 3-0 SILK 18"/HS-24 FDA UDI
- Description
- SUTURE 3-0 SILK 18"/HS-24 FDA UDI
Identifiers
- Catalog Number
- B64E FDA UDI
- Primary DI / UDI-DI
- B070B64E0 FDA UDI
- FDA Product Code
- GAP FDA UDI
- GMDN Term
- Silk suture FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Silk suture
Havel's by Havel's Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Silk suture.
- Sofsilk — Covidien LP · Class II
- PERMA-HAND — Ethicon Inc. · Class II
- DemeSILK — DemeTECH Corp · Class II
- DemeSILK — DemeTECH Corp · Class II
- DemeSILK — DemeTECH Corp · Class II
- Sofsilk — Covidien LP · Class II
- DemeSILK — DemeTECH Corp · Class II
- DemeSILK — DemeTECH Corp · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Havel's Incorporated
Sources (1)
- FDA UDI 28d12bf7-a523-4757-a4b2-c8145f9fd77f 35 fields · synced May 31, 2026