← Back to catalogue

MIN-R EV Film

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
MIN-R EV Film FDA UDI
Generic Name
Medical x-ray film, screen FDA UDI
Device Name
MIN-R EV FILM 24X30CM 100SH FDA UDI
Model / Reference
MIN-R EV Film FDA UDI
Description
MIN-R EV FILM 24X30CM 100SH FDA UDI

Identifiers

Catalog Number
1851609 FDA UDI
Primary DI / UDI-DI
40889971851600 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
Medical x-ray film, screen FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1840 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical x-ray film, screen

MIN-R EV Film by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical x-ray film, screen.

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

Sources (1)

  • FDA UDI 68a7d4a3-99b3-41af-ac43-9ada96213a5a 35 fields · synced Jun 8, 2026