← Back to catalogue

MIN-R 2 Cassette with MIN-R 2190 Screen

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
MIN-R 2 Cassette with MIN-R 2190 Screen FDA UDI
Generic Name
X-ray intensifying screen FDA UDI
Device Name
18x24 MIN-R 2 CASS W/ MIN-R 2190 SCREEN FDA UDI
Model / Reference
MIN-R 2 Cassette with MIN-R 2190 Screen FDA UDI
Description
18x24 MIN-R 2 CASS W/ MIN-R 2190 SCREEN FDA UDI

Identifiers

Catalog Number
8604555 FDA UDI
Primary DI / UDI-DI
60889978604555 FDA UDI
FDA Product Code
EAM FDA UDI
IXA FDA UDI
GMDN Term
X-ray intensifying screen FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1960 FDA UDI
892.1850 FDA UDI
Commercial Distribution
Not 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

MIN-R 2 Cassette with MIN-R 2190 Screen by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Carestream Health, Inc.

Sources (1)

  • FDA UDI ff1ccbb7-7215-4909-97e8-76159c6413c9 35 fields · synced Jun 8, 2026