Primary Device ID | 00630414585475 |
NIH Device Record Key | af03bd08-1b76-4503-bddd-f554a3b37789 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ADVIA Centaur® XP Analyzer |
Version Model Number | 10471899 |
Catalog Number | 078-A011R03 |
Company DUNS | 064608573 |
Company Name | Siemens Healthcare Diagnostics Inc. |
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 | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00630414585475 [Primary] |
JJE | ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-01-01 |
Device Publish Date | 2018-12-01 |
00630414585475 | ADVIA® CENTAUR® XP Refurbished Instrument |
00630414573564 | ADVIA® CENTAUR® XP Instrument |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ADVIA CENTAUR 75658644 2427460 Live/Registered |
SIEMENS HEALTHCARE DIAGNOSTICS INC. 1999-03-11 |