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Precision Cut GafChromic™ Film

FDA UDI

Class I (US FDA UDI)

by Sun Nuclear Corporation

Identity

Trade Name
Precision Cut GafChromic™ Film FDA UDI
Generic Name
Medical x-ray film, non-screen FDA UDI
Device Name
Radiographic film FDA UDI
Model / Reference
1582 FDA UDI
Description
Radiographic film FDA UDI

Identifiers

Primary DI / UDI-DI
05060608881512 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical x-ray film, non-screen

Precision Cut GafChromic™ Film by Sun Nuclear Corporation — 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

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Manufacturer

Sources (1)

  • FDA UDI b3f46b5c-fa0f-4782-b247-b937bed6f4d9 34 fields · synced Jun 8, 2026