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KMI IMI Group

FDA UDI

Class I (US FDA UDI)

by Innovative Med, Inc.

Identity

Trade Name
KMI IMI Group FDA UDI
Generic Name
Liposuction system cannula, single-use FDA UDI
Device Name
Disposable Micro Injection Needle FDA UDI
Model / Reference
19-0099 FDA UDI
Description
Disposable Micro Injection Needle FDA UDI

Identifiers

Primary DI / UDI-DI
00851314007212 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Liposuction system cannula, single-use 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Liposuction system cannula, single-use

KMI IMI Group by Innovative Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c937a889-454f-4978-a6fd-d5b33b96cab0 34 fields · synced Jun 8, 2026