Identity
- Trade Name
- ADC® FDA UDI
- Generic Name
- Ring cutter FDA UDI
- Device Name
- Ring Cutter Replacement Blade, FDA UDI
- Model / Reference
- 381 FDA UDI
- Description
- Ring Cutter Replacement Blade, FDA UDI
Identifiers
- Catalog Number
- 381 FDA UDI
- Primary DI / UDI-DI
- 00634782001889 FDA UDI
- FDA Product Code
- FNS FDA UDI
- GMDN Term
- Ring cutter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6200 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
No
FDA UDI
Over-the-Counter
Yes
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
Category: Ring cutter
Adc® by American Diagnostic Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ring cutter.
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
- Beaver® — Beaver-Visitec International, Inc. · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- American Diagnostic Corporation
Sources (1)
- FDA UDI d0f8b2c8-0d35-4ea0-81e0-315278d14648 35 fields · synced May 30, 2026