| Primary Device ID | B0991627000 |
| NIH Device Record Key | cb108852-6b70-449a-a1e0-bd77677dc9e3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MCPHERSON BIPOLAR FORCEPS |
| Version Model Number | 16-2700 |
| 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 | 8008217496 |
| INFO@SONTECINSTRUMENTS.COM | |
| Phone | 8008217496 |
| INFO@SONTECINSTRUMENTS.COM | |
| Phone | 8008217496 |
| INFO@SONTECINSTRUMENTS.COM |
| Length | 94 Millimeter |
| Length | 94 Millimeter |
| Length | 94 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896000247 [Primary] |
| HIBCC | B0991627000 [Previous] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B0991627000]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B0991627000]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B0991627000]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-10-28 |
| Device Publish Date | 2018-08-20 |
| B0991627100 | MCPHERSON BIPOLAR FORCEPS ANGLED TYPE PLATFORM |
| B0991627000 | MCPHERSON BIPOLAR FORCEPS SMOOTH TYING PLATFORM STRAIGHT TIP |