| Primary Device ID | 00192896116405 |
| NIH Device Record Key | a54ad1e7-e2e2-4a29-8a21-7b1d3390c7e2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Severin Lacrimal Cannula |
| Version Model Number | 1103-500HS |
| Catalog Number | 1103-500HS |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)821-7496 |
| info@sontecinstruments.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896116405 [Primary] |
| HMX | Cannula, ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896116405]
Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-19 |
| Device Publish Date | 2024-02-09 |
| 00192896083141 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896083134 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896083127 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896053205 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896053199 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896053182 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896053175 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896053168 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896053151 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896052291 | SEVERIN LACRIMAL CANNULA CURVED TIP |
| 00192896116405 | Severin Lacrimal Cannula Straight Tip 27 Gauge |