| Primary Device ID | 00192896089419 |
| NIH Device Record Key | ea0db1e9-7d92-4b50-8015-89d6828b37f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ALLIGATOR FORCEPS |
| Version Model Number | 1271-012Q |
| Catalog Number | 1271-012Q |
| 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 | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com | |
| Phone | +1(800) 821-7496 |
| info@sontecinstruments.com |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Length | 6.5 Inch |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896089419 [Primary] |
| FCL | FORCEPS, BIOPSY, NON-ELECTRIC |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-03 |
| Device Publish Date | 2018-10-24 |
| 00192896089419 | ALLIGATOR FORCEPS DELICATE TUBULAR SHAFT |
| 00192896079953 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE DUST SIDE BITING JAW |
| 00192896056312 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
| 00192896056305 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
| 00192896056299 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
| 00192896056282 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
| 00192896041370 | ALLIGATOR FORCEPS MICROSCOPIC WITH LOCK SERRATED JAW BLACK ANODIZED COATED |
| 00192896041202 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE SIDE BITING JAW |
| 00192896041196 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE SIDE BITING JAW |
| 00192896095472 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE SERRATED TIP SIDE BITER |
| 00192896093478 | ALLIGATOR FORCEPS SIDE BITER TUNGSTEN CARBIDE SERRATED TIP |