| Primary Device ID | B09927009450 |
| NIH Device Record Key | e456c9b0-7cf6-419c-8525-55054b73bf8b |
| Commercial Distribution Discontinuation | 2018-06-22 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | BIPOLAR SCOVILLE GREENWOOD BAYONET FORCEPS |
| Version Model Number | 2700-945 |
| 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 |
| Length | 7.75 Inch |
| Device Size Text, specify | 0 |
| Length | 7.75 Inch |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B09927009450 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B09927009450]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09927009450]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 7 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-10-14 |
| B0992700968NS0 | BIPOLAR SCOVILLE GREENWOOD BAYONET FORCEPS FLAT HANDLE NON-STICK |
| B09927009450 | BIPOLAR SCOVILLE GREENWOOD BAYONET FORCEPS IRRIGATION INSULATION STRAIGHT |