| Primary Device ID | B09921001430 |
| NIH Device Record Key | bf63b97a-3eb5-4b49-b68f-6b9ab6c19151 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | COOLEY SUBRAMANIAN AORTIC CLAMP |
| Version Model Number | 2100-143 |
| Company DUNS | 040729840 |
| Company Name | SONTEC INSTRUMENTS, 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 | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 8008217496 |
| INFO@SONTECINSTRUMENTS.COM | |
| Phone | 8008217496 |
| INFO@SONTECINSTRUMENTS.COM | |
| Phone | 8008217496 |
| INFO@SONTECINSTRUMENTS.COM |
| Length | 6.25 Inch |
| Length | 6.25 Inch |
| Length | 6.25 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896010086 [Primary] |
| HIBCC | B09921001430 [Previous] |
| DXC | Clamp, Vascular |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B09921001430]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09921001430]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09921001430]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-08-21 |
| Device Publish Date | 2018-08-24 |
| B09921001450 | COOLEY SUBRAMANIAN AORTIC CLAMP ANGLED JAW |
| B09921001430 | COOLEY SUBRAMANIAN AORTIC CLAMP ANGLED JAW |