Primary Device ID | 00884838090705 |
NIH Device Record Key | 9326ff44-8ce8-4d89-91ac-b28f5cc20522 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DigitalDiagnost C90 |
Version Model Number | 712035 |
Company DUNS | 314101218 |
Company Name | Philips Medical Systems DMC GmbH |
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 | false |
Device Combination Product | true |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx | |
Phone | +1(800)722-9377 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838090705 [Primary] |
MQB | Solid state x-ray imager (flat panel/digital imager) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2019-03-28 |
00884838090705 | Solid State X-Ray Imager (Flat Panel/Digital Imager) |
00884838090699 | Solid State X-Ray Imager (Flat Panel/Digital Imager) |