Primary Device ID | 00192896083141 |
NIH Device Record Key | 09f816e7-78bf-4c60-858c-7d787eeaf5f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SEVERIN LACRIMAL CANNULA |
Version Model Number | 1103-500G |
Catalog Number | 1103-500G |
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 |
Needle Gauge | 26 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896083141 [Primary] |
HMX | Cannula, ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896083141]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-06-12 |
Device Publish Date | 2018-09-21 |
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 |