| Primary Device ID | 00192896094611 |
| NIH Device Record Key | 87762794-9410-47cd-960a-e0ad8c5a1a4f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DORSEY GRASPING FORCEPS |
| Version Model Number | 2901-218S |
| Catalog Number | 2901-218S |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896094611 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896094611]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-04-26 |
| Device Publish Date | 2019-03-07 |
| 00192896094611 | DORSEY GRASPING FORCEPS DOUBLE ACTION FENESTRATED JAW |
| 00192896110588 | Dorsey Grasping Forceps Fenestrated Single Action Jaw Diameter 5 Millimeter Tube |
| 00192896110571 | Dorsey Grasping Forceps Fenestrated Single Action Jaw 5 Millimeter Diameter Tube |