| Primary Device ID | 00192896079199 |
| NIH Device Record Key | d009d71f-3835-4ecd-85ee-fcabd2257233 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BAYONET CURETTE |
| Version Model Number | 413-051 |
| Catalog Number | 413-051 |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896079199 [Primary] |
| HXB | PROBE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896079199]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-09-10 |
| Device Publish Date | 2018-09-20 |
| 00192896079199 | BAYONET CURETTE DOWN ANGLE RING TIP TITANIUM |
| 00192896079182 | BAYONET CURETTE UP-ANGLE RING TIP TITANIUM |
| 00192896036758 | BAYONET CURETTE BENDING HYPOPHYSIS ENUCLEATOR TITANIUM |
| 00192896104136 | Bayonet Curette Knurled Handle 45 Degree Up Angle Titanium |
| 00192896104853 | Bayonet Curette Knurl Handle 45 Degrees Up Angle Titanium |
| 00192896104846 | Bayonet Curette Knurl Handle 90 Degree Up AngleTitanium |