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Lf

FDA UDI

Class II (US FDA UDI)

by Liebel-Flarsheim Company, LLC

Identity

Trade Name
LF FDA UDI
Generic Name
Angiography contrast medium injection system, line-powered, stationary FDA UDI
Device Name
Angiomat Illumena Hand Button Start Switch (Accessory) FDA UDI
Model / Reference
900211 FDA UDI
Description
Angiomat Illumena Hand Button Start Switch (Accessory) FDA UDI

Identifiers

Primary DI / UDI-DI
10746190004868 FDA UDI
510(k) Number
K963071 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Angiography contrast medium injection system, line-powered, stationary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 39 Feet FDA UDI
Length — 12 Meter FDA UDI

Category: Angiography contrast medium injection system, line-powered, stationary

Lf by Liebel-Flarsheim Company, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiography contrast medium injection system, line-powered, stationary.

Cleared under the same submission

K963071 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Liebel-Flarsheim Company, LLC

Sources (1)

  • FDA UDI b4a26e30-609e-4d00-a4ac-ded35da32710 35 fields · synced May 30, 2026