Primary Device ID | 00192896054042 |
NIH Device Record Key | 2a1860f2-e403-4279-ae06-e13d31fd3f2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEXAGONAL SCREWDRIVER |
Version Model Number | 1106-258 |
Catalog Number | 1106-258 |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896054042 [Primary] |
HXX | SCREWDRIVER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896054042]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-12 |
Device Publish Date | 2018-09-11 |
00192896054073 | HEXAGONAL SCREWDRIVER PHENOLIC HANDLE |
00192896054066 | HEXAGONAL SCREWDRIVER PHENOLIC HANDLE |
00192896054042 | HEXAGONAL SCREWDRIVER PHENOLIC HANDLE |
00192896102101 | HEXAGONAL SCREWDRIVER PHENOLIC HANDLE |