Identity
- Trade Name
- Trinity Sterile, Inc. FDA UDI
- Generic Name
- Suture removal kit FDA UDI
- Device Name
- SUTURE REMOVAL TRAY FDA UDI
- Model / Reference
- 80359 FDA UDI
- Description
- SUTURE REMOVAL TRAY FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10841767104870 FDA UDI
- FDA Product Code
- MCZ FDA UDI
- GMDN Term
- Suture removal kit 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Suture removal kit
Trinity Sterile, Inc. by Trinity Sterile, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suture removal kit.
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- Dukal — Dukal LLC · Class I
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class I
- Centurion — Centurion Medical Products · Class I
- Custom Healthcare Systems Inc. — Manus Medical, LLC · Class I
- Custom Healthcare Systems Inc. — Manus Medical, LLC · Class I
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class I
- Centurion — Centurion Medical Products · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Trinity Sterile, Inc.
Sources (1)
- FDA UDI 014e8e0d-1478-4459-85a5-125e9e25130e 33 fields · synced Jun 1, 2026