CURIX ORTHO REGULAR 3KUBW

GUDID 05414904033883

CURIX CAS US+OR REG 30X35

AGFA

X-ray film cassette, manual
Primary Device ID05414904033883
NIH Device Record Key07574081-8a0e-404e-9507-0f184daacfef
Commercial Distribution StatusIn Commercial Distribution
Brand NameCURIX ORTHO REGULAR
Version Model NumberCURIX ORTHO REGULAR 30X35
Catalog Number3KUBW
Company DUNS374444883
Company NameAGFA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(877)777-2432
Emailsalesinfo@agfa.com

Device Dimensions

Length30 Centimeter
Length30 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS105414904033883 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IXACassette, radiographic film

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-06-14
Device Publish Date2016-09-01

On-Brand Devices [CURIX ORTHO REGULAR]

05414904036693CURIX CAS US+OR REG 35X35
05414904034606CURIX CAS EU+OR REG 30X40
05414904034590CURIX CAS EU+OR REG 24X30
05414904034576CURIX CAS EU+OR REG 18X43
05414904034569CURIX CAS EU+OR REG 18X24
05414904033890CURIX CAS US+OR REG 30X40
05414904033883CURIX CAS US+OR REG 30X35
05414904033876CURIX CAS US+OR REG 24X30
05414904033760CURIX CAS US+OR REG 18X24
05414904033036CURIX CAS EU+OR REG 35X43
05414904033029CURIX CAS EU+OR REG 35X35
05414904006511CURIX CAS EU+OR REG 15X30

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