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Precision Cut EBT3 GafChromic™ Film

FDA UDI

Class I (US FDA UDI)

by Sun Nuclear Corporation

Identity

Trade Name
Precision Cut EBT3 GafChromic™ Film FDA UDI
Generic Name
Medical x-ray film, non-screen FDA UDI
Device Name
Precision Cut EBT3 GafChromic™ Film FDA UDI
Model / Reference
158200 FDA UDI
Description
Precision Cut EBT3 GafChromic™ Film FDA UDI

Identifiers

Primary DI / UDI-DI
05060608881178 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
Not 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Precision Cut EBT3 GafChromic™ Film by Sun Nuclear Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 241534ad-c657-4676-84ff-ffe60f8f35e8 34 fields · synced Jun 8, 2026