| Primary Device ID | B09926002340 |
| NIH Device Record Key | 536c9687-c898-4726-bde0-4577641345e1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TITANIUM SATINSKY VENA CAVA CLAMP |
| Version Model Number | 2600-234 |
| Catalog Number | 2600-234 |
| 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 | true |
| 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 | 800-821-7496 |
| info@sontecinstruments.com | |
| Phone | 800-821-7496 |
| info@sontecinstruments.com | |
| Phone | 800-821-7496 |
| info@sontecinstruments.com |
| Length | 10 Inch |
| Length | 10 Inch |
| Length | 10 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896004832 [Primary] |
| HIBCC | B09926002340 [Previous] |
| DXC | Clamp, Vascular |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B09926002340]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09926002340]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09926002340]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-08-21 |
| Device Publish Date | 2018-08-20 |
| B09926002340 | TITANIUM SATINSKY VENA CAVA CLAMP SMALL |
| B09926002320 | TITANIUM SATINSKY VENA CAVA CLAMP MEDIUM |
| B09926002300 | TITANIUM SATINSKY VENA CAVA CLAMP LARGE |