| Primary Device ID | 00888937027808 |
| NIH Device Record Key | 933cda0c-4694-472a-b5a6-aeed70427e22 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CooperSurgical® |
| Version Model Number | DP-CAB01 |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888937027808 [Primary] |
| JOP | Transducer, Ultrasonic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-02 |
| Device Publish Date | 2026-01-23 |
| 00888937027822 | Doppler Blood Flow Monitor |
| 00888937027808 | Doppler Extension Cable |
| 00888937027792 | Swartz Doppler Probe |
| 00888937027785 | Swartz Doppler Long Cuff Probe |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() COOPERSURGICAL 85186600 4058824 Live/Registered |
CooperSurgical, Inc. 2010-11-29 |
![]() COOPERSURGICAL 74219286 1862209 Live/Registered |
COOPERSURGICAL, INC. 1991-11-06 |