| Primary Device ID | 00192896100510 |
| NIH Device Record Key | 3c3077ca-4489-4392-b529-440de9e82f9a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOPSY CUP |
| Version Model Number | 2901-123 |
| 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 | +1(800)821-7496 |
| info@sontecinstruments.com |
| Stent Length | 360 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896100510 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896100510]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-03-03 |
| Device Publish Date | 2020-02-24 |
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| B0992901111S0 | BIOPSY CUP WITHOUT THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| B0992901111L0 | BIOPSY CUP WITHOUT THORN DOUBLE-ACTION JAWS FOR TUBE SHAFT |
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| 00192896100510 | BIOPSY CUP DOUBLE ACTION JAWS FOR 0.5 MILLIMETER TUBE |