| Primary Device ID | 00192896049369 |
| NIH Device Record Key | afce2028-b591-409d-a5da-b7cf4679bdec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SENN RETRACTOR |
| Version Model Number | 1100-668 |
| Catalog Number | 1100-668 |
| 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 | 6.25 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896049369 [Primary] |
| FFO | RETRACTOR, SELF-RETAINING |
| GAD | Retractor |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896049369]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-05-22 |
| Device Publish Date | 2018-09-14 |
| 00192896092297 | SENN RETRACTOR BLUNT TIP BLUE ELECTRO COATED |
| 00192896092280 | SENN RETRACTOR SHARP TIP BLUE ELECTRO COATED |
| 00192896076990 | SENN RETRACTOR DOUBLE ENDED BLUNT TIP |
| 00192896076983 | SENN RETRACTOR DOUBLE ENDED SHARP TIP |
| 00192896049376 | SENN RETRACTOR BLUNT TIPS |
| 00192896049369 | SENN RETRACTOR SHARP TIPS |
| 00192896112735 | Senn Retractor Sharp Titanium |
| 00192896121690 | Senn Retractor Blunt Quantum |
| 00192896121683 | Senn Retractor Sharp Quantum |