| Primary Device ID | B09926050900 |
| NIH Device Record Key | cd3f460b-867f-48d0-a259-515adba38b01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TITANIUM KITZMILLER CLAMP |
| Version Model Number | 2605-090 |
| 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 | 4.5 Inch |
| Length | 4.5 Inch |
| Length | 4.5 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896005044 [Primary] |
| HIBCC | B09926050900 [Previous] |
| DXC | Clamp, Vascular |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B09926050900]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09926050900]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09926050900]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-08-21 |
| Device Publish Date | 2018-08-20 |
| B09926055060 | TITANIUM KITZMILLER CLAMP COOLEY JAWS ANGLED RIGHT |
| B09926050920 | TITANIUM KITZMILLER CLAMP RIGHT |
| B09926050900 | TITANIUM KITZMILLER CLAMP LEFT |
| B09926055070 | TITANIUM KITZMILLER CLAMP COOLEY JAWS ANGLED LEFT |