Identity
- Trade Name
- Micro-Forceps CROSS MAX FDA UDI
- Generic Name
- Surgical A/V-shaped microvessel clamp FDA UDI
- Model / Reference
- 30-0702 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00883475953176 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Surgical A/V-shaped microvessel clamp FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 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
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: Surgical A/V-shaped microvessel clamp
Micro-Forceps CROSS MAX by Charmant Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical A/V-shaped microvessel clamp.
- LAZIC — Peter Lazic GmbH · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- LAZIC — Peter Lazic 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Charmant Inc.
Sources (1)
- FDA UDI ff1e1db6-d534-4e6c-9fb6-06becd786cd6 32 fields · synced May 30, 2026