Primary Device ID | 00192896075023 |
NIH Device Record Key | aa12866d-ffb9-4766-9ef2-7425fe1db4fe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GILLS-WELSH ASPRIRATING CANNULA |
Version Model Number | 16-5660 |
Catalog Number | 16-5660 |
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 | 25 Gauge |
Needle Gauge | 25 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896075023 [Primary] |
HMX | Cannula, ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896075023]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-22 |
Device Publish Date | 2018-09-20 |
00192896075047 | GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP |
00192896075030 | GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP |
00192896075023 | GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP |