Identity
- Trade Name
- Anastoclip Atraumatic Forceps FDA UDI
- Generic Name
- Clip forceps FDA UDI
- Device Name
- Anastoclip Atraumatic Forceps, 20cm FDA UDI
- Model / Reference
- 4001-07 FDA UDI
- Description
- Anastoclip Atraumatic Forceps, 20cm FDA UDI
Identifiers
- Catalog Number
- 4001-07 FDA UDI
- Primary DI / UDI-DI
- 00840663107285 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Clip forceps 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Clip forceps
Anastoclip Atraumatic Forceps by LeMaitre Vascular, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Clip forceps.
- Anastoclip Atraumatic Forceps — LeMaitre Vascular, 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
- LeMaitre Vascular, Inc.
Sources (1)
- FDA UDI af8a5d31-a2d8-4257-a06a-98f89623dd6f 35 fields · synced Jun 9, 2026