| Primary Device ID | 00192896023222 |
| NIH Device Record Key | d57facfc-8567-4762-b3f0-03dfa4e9aa99 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SEMKEN TISSUE FORCEPS |
| Version Model Number | 136-708 |
| Catalog Number | 136-708 |
| Company DUNS | 040729840 |
| Company Name | SONTEC INSTRUMENTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | +1(800) 821-7496 |
| info@sontecinstruments.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896023222 [Primary] |
| HTD | FORCEPS |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896023222]
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 | 2018-09-11 |
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| 00192896076495 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
| 00192896076471 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
| 00192896076464 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
| 00192896076297 | SEMKEN TISSUE FORCEPS DELICATE TIP |
| 00192896023222 | SEMKEN TISSUE FORCEPS |
| 00192896023215 | SEMKEN TISSUE FORCEPS |
| 00192896121218 | Semken Tissue Forceps With Tungsten Carbide Serrated Platform 1x2 Teeth |