| Primary Device ID | 00827002266155 |
| NIH Device Record Key | d239e001-d23a-4a52-ad73-5ba0b5f4af5e |
| Commercial Distribution Discontinuation | 2019-08-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Pivet |
| Version Model Number | G26615 |
| Catalog Number | K-PAI-1000 |
| Company DUNS | 042823948 |
| Company Name | COOK INCORPORATED |
| 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 | true |
| 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(812)330-5494 |
| sharedservices@cookmedical.com |
| Special Storage Condition, Specify | Between 0 and 0 *Store in dark, dry, cool place. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00827002266155 [Primary] |
| MFD | CANNULA, INTRAUTERINE INSEMINATION |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-09-02 |
| Device Publish Date | 2016-09-24 |
| 00827002304574 | Pivet Embryo Transfer Catheter Set |
| 00827002266155 | Pivet Insemination Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PIVET 88712317 not registered Live/Pending |
Pivet Communications, LLC 2019-12-02 |
![]() PIVET 88712270 not registered Live/Pending |
Pivet Communications, LLC 2019-12-02 |
![]() PIVET 88641474 not registered Live/Pending |
Cox Automotive, Inc. 2019-10-03 |