Identity
- Trade Name
- Reicodent FDA UDI
- Generic Name
- Suture scissors FDA UDI
- Device Name
- Ligature scissors 9 cm REGULAR CUT curved FDA UDI
- Model / Reference
- 02-1191-1 FDA UDI
- Description
- Ligature scissors 9 cm REGULAR CUT curved FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04061644046751 FDA UDI
- FDA Product Code
- LRW FDA UDI
- GMDN Term
- Suture scissors 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
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
Moist Heat or Steam Sterilization FDA UDI
Category: Suture scissors
Reicodent by devemed GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suture scissors.
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- Sklar® — Sklar Corporation · Class I
- Quinelato — Schobell Industrial Ltda · Class I
- Rocket — Rocket Medical Plc
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- STOMA® — Storz am Mark GmbH · 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
- devemed GmbH
Sources (1)
- FDA UDI 6dcfc94a-0705-407a-a989-73d99ad4453b 34 fields · synced Jun 8, 2026