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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, reusable FDA UDI
Device Name
Infiltration Cannula FDA UDI
Model / Reference
19-0091 FDA UDI
Description
Infiltration Cannula FDA UDI

Identifiers

Primary DI / UDI-DI
00851314007106 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Liposuction system cannula, reusable 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

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, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 410439d1-a8bb-44f4-9a66-162e1ed5d802 34 fields · synced May 31, 2026