Primary Device ID | 00192896082571 |
NIH Device Record Key | ac7920a3-1803-4a7e-a26d-a343e051399f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WIRE END CUTTER |
Version Model Number | 1103-100Q |
Catalog Number | 1103-100Q |
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 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Size Text, specify | 0 |
Length | 8.5 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896082571 [Primary] |
HXZ | CUTTER, WIRE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896082571]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-06-03 |
Device Publish Date | 2018-09-21 |
00192896082595 | WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE BLADES |
00192896082571 | WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE TIPS |
00192896051522 | WIRE SIDE CUTTER TUNGSTEN CARBIDE BLADES |
00192896051515 | WIRE END CUTTER TUNGSTEN CARBIDE BLADES |
00192896051485 | WIRE END CUTTER DOUBLE SPRING ACTION TUNGSTEN CARBIDE BLADES |
00192896051416 | WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE BLADES |
00192896105195 | WIRE END CUTTER DOUBLE SPRING ACTION TUNGSTEN CARBIDE CUTS WIRE UP TO 1.5 MILLIMETERS 6.25 INCHE |