| Primary Device ID | B09927009300 |
| NIH Device Record Key | 88c44de4-6099-4198-bd64-4122d799dae4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIPOLAR COAPTATION FORCEPS |
| Version Model Number | 2700-930 |
| 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 | 4.25 Inch |
| Length | 4.25 Inch |
| Length | 4.25 Inch |
| Length | 4.25 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896100459 [Primary] |
| HIBCC | B09927009300 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B09927009300]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09927009300]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-14 |
| Device Publish Date | 2020-01-06 |
| 00192896010802 | BIPOLAR COAPTATION FORCEPS INSULATED |
| B09927009300 | BIPOLAR COAPTATION FORCEPS |