Primary Device ID | 20888937003776 |
NIH Device Record Key | 9ee030ac-fec6-49cc-8e12-a348a9d5e2f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fischer Cone Biopsy Excisor |
Version Model Number | 900-158 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888937003772 [Primary] |
GS1 | 20888937003776 [Package] Contains: 00888937003772 Package: [5 Units] In Commercial Distribution |
HGI | Electrocautery, Gynecologic (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-08-16 |
20888937003776 | Fischer Cone Biopsy Excisor; Small Wide Angle Extended |
20888937003769 | Fischer Cone Biopsy Excisor; Small Wide Angle |
20888937003745 | Fischer Cone Biopsy Excisor; Large Shallow |
20888937003738 | Fischer Cone Biopsy Excisor; Medium Extended |
20888937003721 | Fischer Cone Biopsy Excisor; Large |
20888937003714 | Fischer Cone Biopsy Excisor; Medium |
20888937003707 | Fischer Cone Biopsy Excisor; Small |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FISCHER CONE BIOPSY EXCISOR 85466592 4270743 Live/Registered |
CooperSurgical, Inc. 2011-11-07 |