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Curix Ortho Fast

FDA UDI

Class II (US FDA UDI)

by Agfa Corp.

Identity

Trade Name
CURIX ORTHO FAST FDA UDI
Generic Name
X-ray film cassette, manual FDA UDI
Device Name
CURIX CAS EU+OR FAST 35X43 FDA UDI
Model / Reference
CURIX ORTHO FAST 35X43 FDA UDI
Description
CURIX CAS EU+OR FAST 35X43 FDA UDI

Identifiers

Catalog Number
3KOS5 FDA UDI
Primary DI / UDI-DI
05414904033364 FDA UDI
510(k) Number
K023020 FDA UDI
FDA Product Code
IXA FDA UDI
GMDN Term
X-ray film cassette, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1850 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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 35 Centimeter FDA UDI
Width — 43 Centimeter FDA UDI

Category: X-ray film cassette, manual

Curix Ortho Fast by Agfa Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette, manual.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agfa Corp.

Sources (1)

  • FDA UDI 93f62ee2-543a-4acb-b1a8-97feab517e25 37 fields · synced Jun 6, 2026