Primary Device ID | 00192896012431 |
NIH Device Record Key | 7ec99e6a-0d7b-4556-93c8-c40dbcb8aa5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GIL-VERNET RETRACTOR |
Version Model Number | 10-4241 |
Catalog Number | 10-4241 |
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 | 5.75 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896012431 [Primary] |
HNI | Retractor, ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896012431]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-05-14 |
Device Publish Date | 2018-09-12 |
00192896086876 | GIL-VERNET RETRACTOR |
00192896086869 | GIL-VERNET RETRACTOR |
00192896012431 | GIL-VERNET RETRACTOR OPEN BLADE FENESTRATED TIP SIZE 4 |
00192896012394 | GIL-VERNET RETRACTOR OPEN BLADE FENESTRATED TIP SIZE 3 |
00192896012356 | GIL-VERNET RETRACTOR OPEN BLADE FENESTRATED TIP SIZE 2 |
00192896012301 | GIL-VERNET RETRACTOR OPEN BLADE FENESTRATED TIP SIZE 1 |
00192896101944 | Gil-Vernet Retractor Fenestrated Open Blade |
00192896101937 | Gil-Vernet Retractor Fenestrated Open Blade |
00192896101920 | Gil-Vernet Retractor Fenestrated Open Blade |
00192896101913 | Gil-Vernet Retractor Fenestrated Open Blade |
00192896108370 | Gil-Vernet Retractor 15 Millimeter Round Blade |