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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
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Manual infusion tubing w/ Luer Lock & IV Bag Spike FDA UDI
Model / Reference
ITD FDA UDI
Description
Manual infusion tubing w/ Luer Lock & IV Bag Spike FDA UDI

Identifiers

Catalog Number
IM-ITD FDA UDI
Primary DI / UDI-DI
00851314007168 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Surgical irrigation/aspiration tubing set

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

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 35a552d0-b8e4-45f7-88d2-ebfa7c4c12f5 35 fields · synced May 30, 2026