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LipiVage®

FDA UDI

Class II (US FDA UDI)

by Genesis Biosystems, Inc.

Identity

Trade Name
LipiVage® FDA UDI
Generic Name
Irrigation syringe FDA UDI
Device Name
LipiVage Harvester with cannula FDA UDI
Model / Reference
D11-0290-109 FDA UDI
Description
LipiVage Harvester with cannula FDA UDI

Identifiers

Primary DI / UDI-DI
00818257020029 FDA UDI
FDA Product Code
MUU FDA UDI
QKL FDA UDI
GMDN Term
Irrigation syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Irrigation syringe

LipiVage® by Genesis Biosystems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Irrigation syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12950e1f-131a-49b7-b224-0a242f134862 34 fields · synced May 30, 2026