Primary Device ID | 50888937011284 |
NIH Device Record Key | 045680b9-397d-4259-aea9-2d54ccdb3b2f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Papette |
Version Model Number | 908002 |
Company DUNS | 801895244 |
Company Name | Coopersurgical, 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 | true |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 50888937011284 [Primary] |
HHT | Spatula, Cervical, Cytological |
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 | 2016-10-14 |
20888937011320 | WALLACH Papette® (Non-Sterile) Cervical Cell Sampler |
20888937011313 | WALLACH Papette® (Non-Sterile) Cervical Cell Sampler |
20888937011306 | WALLACH Papette® (Non-sterile) Cervical Cell Sampler |
20888937011290 | WALLACH Papette® (Non-Sterile) Cervical Cell Sampler |
50888937011284 | WALLACH Papette |
50888937011277 | WALLACH Papette® (Non-Sterile) For Cervical Cytology utilizing the Conventional Pap Smear |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PAPETTE 78391186 2954995 Live/Registered |
COOPERSURGICAL, INC. 2004-03-26 |
PAPETTE 72242274 0832891 Dead/Expired |
ORTHO PHARMACEUTICAL CORPORATION 1966-03-30 |