← Back to catalogue

GAFchromic™

FDA UDI

Class I (US FDA UDI)

by Ashland Specialty Ingredients, G.P.

Identity

Trade Name
GAFchromic™ FDA UDI
Generic Name
Medical x-ray film, non-screen FDA UDI
Model / Reference
EBT3 MX-HD BLCK-2D ANT FDA UDI

Identifiers

Catalog Number
970000 FDA UDI
Primary DI / UDI-DI
00850000065611 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
Medical x-ray film, non-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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical x-ray film, non-screen

GAFchromic™ by Ashland Specialty Ingredients, G.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical x-ray film, non-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 f58797b2-c784-4bad-9762-1001b762adb4 33 fields · synced Jun 9, 2026