Identity
- Trade Name
- Laschal Surgical FDA UDI
- Generic Name
- Silk suture FDA UDI
- Device Name
- Silk Suture. Reverse Cutting. 4-0 19mm FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Silk Suture. Reverse Cutting. 4-0 19mm FDA UDI
Identifiers
- Catalog Number
- S-4019 FDA UDI
- Primary DI / UDI-DI
- B659S40190 FDA UDI
- FDA Product Code
- LRW FDA UDI
- GMDN Term
- Silk suture 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Silk suture
Laschal Surgical by LASCHAL SURGICAL Instruments, LLC — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- LASCHAL SURGICAL Instruments, LLC
Sources (1)
- FDA UDI 180154a8-7671-44da-9d92-3f6aa0fc293a 34 fields · synced May 30, 2026