Identity
- Trade Name
- LipoGrafter FDA UDI
- Generic Name
- General-purpose syringe, single-use FDA UDI
- Device Name
- The LipoGrafter kit is a sterile, single use disposable device that is used in harvesting, sedimenting, and transferring autologous fat to the desired anatomy. FDA UDI
- Model / Reference
- 913000 FDA UDI
- Description
- The LipoGrafter kit is a sterile, single use disposable device that is used in harvesting, sedimenting, and transferring autologous fat to the desired anatomy. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00859070006050 FDA UDI
- FDA Product Code
- KYZ FDA UDI
- GMDN Term
- General-purpose syringe, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6960 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose syringe, single-use
LipoGrafter by Musculoskeletal Transplant Foundation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General-purpose syringe, single-use.
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- BD Safety-Lok — BECTON DICKINSON AND COMPANY · Class II
- SURGYCO — Surgyco LLC · 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
- Musculoskeletal Transplant Foundation
Sources (1)
- FDA UDI 03dd2c84-d860-4a42-a3d1-4397018cda56 34 fields · synced May 30, 2026