Identity
- Trade Name
- Penditure™ FDA UDI
- Generic Name
- Ligation clip, metallic FDA UDI
- Device Name
- TOOL PENDITURE LAACSIZER FDA UDI
- Model / Reference
- LAACSIZER FDA UDI
- Description
- TOOL PENDITURE LAACSIZER FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000791483 FDA UDI
- FDA Product Code
- FZX FDA UDI
- GMDN Term
- Ligation clip, metallic 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
Yes
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
Category: Ligation clip, metallic
Penditure™ by Medtronic, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ligation clip, metallic.
- WECK — TELEFLEX INCORPORATED · Class II
- WECK — TELEFLEX INCORPORATED · Class II
- DR. POYNTER MC — APPLIED MEDICAL RESOURCES CORP. · Class II
- DR.BRIZENDINE LAP CHOLECYSTECTOMY — APPLIED MEDICAL RESOURCES CORP. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class II
- CLIP 9 VITALITEC — PETERS SURGICAL · Class II
- AtriClip™ LAA Exclusion System — ATRICURE, INC. · Class II
- CONZALVO ROBOTIC SLEEVE — APPLIED MEDICAL RESOURCES CORP. · Class II
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
- Medtronic, Inc.
Sources (1)
- FDA UDI 822678bd-74e8-4495-866d-99e733d597ca 34 fields · synced Jun 8, 2026