| Primary Device ID | 00192896081246 |
| NIH Device Record Key | 719fb085-0be8-461d-a3c1-5834d2f58c86 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DEBAKEY VASCULAR FORCEPS |
| Version Model Number | 1100-182A |
| Catalog Number | 1100-182A |
| 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 | 00192896081246 [Primary] |
| GEN | FORCEPS, GENERAL & PLASTIC SURGERY |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896081246]
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 | 2018-09-20 |
| 00192896081253 | DEBAKEY VASCULAR FORCEPS |
| 00192896081246 | DEBAKEY VASCULAR FORCEPS |
| 00192896081239 | DEBAKEY VASCULAR FORCEPS |
| 00192896067516 | DEBAKEY VASCULAR FORCEPS STRAIGHT FENESTRATED HOLE HANDLE TITANIUM |
| 00192896067493 | DEBAKEY VASCULAR FORCEPS STRAIGHT FENESTRATED HOLE HANDLE TITANIUM |
| 00192896067479 | DEBAKEY VASCULAR FORCEPS STRAIGHT FENESTRATED HOLE HANDLE TITANIUM |
| 00192896046375 | DEBAKEY VASCULAR FORCEPS FENESTRATED HANDLE |
| 00192896121461 | Debakey Vascular Forceps Straight 1.2 Millimeters Tip 6 Hole Handle Titanium |