Primary Device ID | 00884999001732 |
NIH Device Record Key | 4fb5db1f-002f-4a9d-a768-42fabe46a008 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PathVysion |
Version Model Number | 02J01-030 |
Catalog Number | 02J01-030 |
Company DUNS | 878263359 |
Company Name | ABBOTT MOLECULAR 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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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(800)553-7042 |
customerservice@abbottmolecular.com |
Special Storage Condition, Specify | Between 0 and 0 *Protect from light and humidity |
Special Storage Condition, Specify | Between 0 and 0 *Protect from light and humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884999001732 [Primary] |
MVD | SYSTEM, TEST, HER-2/NEU, NUCLEIC ACID OR SERUM |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-11-20 |
00884999001855 | ProbeChek PathVysion HER-2/neu Normal Control Slides |
00884999001831 | ProbeChek PathVysion HER-2/neu Cut-Off Control Slides |
00884999001763 | PathVysion HER-2 DNA Probe Kit |
00884999001756 | PathVysion HER-2 DNA Probe Kit |
00884999001732 | PathVysion HER-2 DNA Probe Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PATHVYSION 75584424 not registered Dead/Abandoned |
Vysis, Inc. 1998-11-06 |
PATHVYSION 75549557 2496630 Live/Registered |
ABBOTT MOLECULAR INC. 1998-09-08 |