| Primary Device ID | 20888937003707 |
| NIH Device Record Key | 23505b7e-4ae8-4f1c-ac55-899480df9d76 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fischer Cone Biopsy Excisor |
| Version Model Number | 900-150 |
| 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 | 00888937003703 [Primary] |
| GS1 | 20888937003707 [Package] Contains: 00888937003703 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 |