Primary Device ID | 05414904033883 |
NIH Device Record Key | 07574081-8a0e-404e-9507-0f184daacfef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CURIX ORTHO REGULAR |
Version Model Number | CURIX ORTHO REGULAR 30X35 |
Catalog Number | 3KUBW |
Company DUNS | 374444883 |
Company Name | AGFA |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(877)777-2432 |
salesinfo@agfa.com |
Length | 30 Centimeter |
Length | 30 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05414904033883 [Primary] |
IXA | Cassette, radiographic film |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-14 |
Device Publish Date | 2016-09-01 |
05414904036693 | CURIX CAS US+OR REG 35X35 |
05414904034606 | CURIX CAS EU+OR REG 30X40 |
05414904034590 | CURIX CAS EU+OR REG 24X30 |
05414904034576 | CURIX CAS EU+OR REG 18X43 |
05414904034569 | CURIX CAS EU+OR REG 18X24 |
05414904033890 | CURIX CAS US+OR REG 30X40 |
05414904033883 | CURIX CAS US+OR REG 30X35 |
05414904033876 | CURIX CAS US+OR REG 24X30 |
05414904033760 | CURIX CAS US+OR REG 18X24 |
05414904033036 | CURIX CAS EU+OR REG 35X43 |
05414904033029 | CURIX CAS EU+OR REG 35X35 |
05414904006511 | CURIX CAS EU+OR REG 15X30 |