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MIN-R 2 Cassette with MIN-R 2000 Screen

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
MIN-R 2 Cassette with MIN-R 2000 Screen FDA UDI
Generic Name
X-ray film cassette, automatic film changing FDA UDI
Device Name
18X24CM MIN-R2 CASS W/MINR 2000 SCR FDA UDI
Model / Reference
MIN-R 2 Cassette with MIN-R 2000 Screen FDA UDI
Description
18X24CM MIN-R2 CASS W/MINR 2000 SCR FDA UDI

Identifiers

Catalog Number
8104101 FDA UDI
Primary DI / UDI-DI
60889978104109 FDA UDI
FDA Product Code
EAM FDA UDI
IXA FDA UDI
GMDN Term
X-ray film cassette, automatic film changing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1960 FDA UDI
892.1850 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

Category: X-ray intensifying screenX-ray film cassette, automatic film changing

MIN-R 2 Cassette with MIN-R 2000 Screen by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette, automatic film changing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02ad29bf-931c-4d2a-b31a-5bd6d9208da1 34 fields · synced Jun 8, 2026