Primary Device ID | 00192896082649 |
NIH Device Record Key | 581934db-46bb-494f-9762-ff87fed683c2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WIRE TWISTER |
Version Model Number | 1103-1506 |
Catalog Number | 1103-1506 |
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 | 6 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896082649 [Primary] |
HXS | TWISTER, WIRE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896082649]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2018-09-21 |
00192896082649 | WIRE TWISTER WITH HOLE NEEDLE HOLDER STYLE COLD COATED HANDLE |
00192896082632 | WIRE TWISTER NEEDLE HOLDER STYLE TUNGSTEN CARBIDE TIPS |
00192896062986 | NEW ORLEANS WIRE TWISTER NEEDLE HOLDER BLUNT TUNGSTEN CARBIDE SERRATED JAW |
00192896062979 | NEW ORLEANS WIRE TWISTER NEEDLE HOLDER BLUNT TUNGSTEN CARBIDE SERRATED JAW |
00192896062962 | NEW ORLEANS WIRE TWISTER NEEDLE HOLDER ROUND TUNGSTEN CARBIDE SERRATED JAW |
00192896062955 | NEW ORLEANS WIRE TWISTER NEEDLE HOLDER ROUND TUNGSTEN CARBIDE SERRATED JAW |
00192896115828 | Wire Twister Tungsten Carbide Serrated Blunt Jaw With Serrated Top |