| Primary Device ID | 00192896090132 |
| NIH Device Record Key | 024945f3-d7fe-404e-8f82-3e376b5d8430 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WILLIGER CURETTE |
| Version Model Number | 467-4133 |
| Catalog Number | 467-4133 |
| 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 |
| Length | 5.5 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896090132 [Primary] |
| HTF | CURETTE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896090132]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-09-10 |
| Device Publish Date | 2018-10-24 |
| 00192896093119 | WILLIGER CURETTE DOUBLE ENDED STRAIGHT # 3-4 |
| 00192896090132 | WILLIGER CURETTE DOUBLE ENDED STRAIGHT TIPS #1-2 |
| 00192896075313 | WILLIGER CURETTE DOUBLE ENDED STRAIGHT TIPS |
| 00192896075306 | WILLIGER CURETTE DOUBLE ENDED ANGLED TIPS |
| 00192896075290 | WILLIGER CURETTE DOUBLE ENDED ANGLED TIPS |
| 00192896020030 | WILLIGER CURETTE DOUBLE ENDED ANGLED #1/2 |
| 00192896020023 | WILLIGER CURETTE DOUBLE ENDED #00/0 |
| 00192896020016 | WILLIGER CURETTE DOUBLE ENDED #0/1 |