| Primary Device ID | 00192896097933 |
| NIH Device Record Key | f4db5479-711c-4211-bc24-1392580d32b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOPSY CUP |
| Version Model Number | 2901-111S |
| Catalog Number | 2901-111S |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 800-821-7496 |
| info@sontecinstruments.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896097933 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896097933]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-07-10 |
| Device Publish Date | 2019-07-02 |
| B0992901113S0 | BIOPSY CUP WITH THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| B0992901113L0 | BIOPSY CUP WITH THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| B09929011130 | BIOPSY CUP WITH THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| B0992901111S0 | BIOPSY CUP WITHOUT THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| B0992901111L0 | BIOPSY CUP WITHOUT THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| 00192896097933 | BIOPSY CUP WITHOUT THORN DOUBLE ACTION |
| 00192896100510 | BIOPSY CUP DOUBLE ACTION JAWS FOR 0.5 MILLIMETER TUBE |