Identity
- Trade Name
- MITRACLIP FDA UDI
- Generic Name
- Cardiovascular implant implantation tool base FDA UDI
- Device Name
- Lift FDA UDI
- Model / Reference
- LFT01ST FDA UDI
- Description
- Lift FDA UDI
Identifiers
- Catalog Number
- LFT01ST FDA UDI
- Primary DI / UDI-DI
- 08717648149580 FDA UDI
- FDA Product Code
- KMK FDA UDI
- GMDN Term
- Cardiovascular implant implantation tool base FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5210 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Cardiovascular implant implantation tool base
Mitraclip by Abbott Vascular — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cardiovascular implant implantation tool base.
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- MITRACLIP — Abbott Vascular · Class I
- MITRACLIP — Abbott Vascular · 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 |
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Manufacturer
- Manufacturer
- Abbott Vascular
Sources (1)
- FDA UDI 42a091f6-5ca5-42c7-ab08-f4fc9a9b9bd5 36 fields · synced May 30, 2026