Primary Device ID | 00192896076570 |
NIH Device Record Key | c832a2e6-f6fc-43e9-9248-ccadcf2fe8f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SKINNER FORCEPS |
Version Model Number | 140-519G |
Catalog Number | 140-519G |
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 | 00192896076570 [Primary] |
HTD | FORCEPS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896076570]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2018-09-20 |
00192896084933 | SKINNER FORCEPS TUNGSTEN CARBIDE SERRATED TIP |
00192896076570 | SKINNER FORCEPS WITH TUNGSTEN CARBIDE PLATFORM SERRATED TIP |
00192896023987 | SKINNER FORCEPS WITH TUNGSTEN CARBIDE SERRATED PLATFORM DELICATE TIP |
00192896023970 | SKINNER FORCEPS WITH TUNGSTEN CARBIDE SERRATED PLATFORM |
00192896023963 | SKINNER FORCEPS WITH TUNGSTEN CARBIDE SERRATED PLATFORM DELICATE TIP |
00192896118478 | Skinner Forceps With Stop Pin Cross-Serrated 1x2 Teeth |
00192896118430 | Skinner Forceps With Stop Pin Cross-Serrated 1x2 Teeth 1.8 Millimeter |
00192896119635 | Skinner Forceps With Stop Pin Cross-Serrated 1x2 Teeth 1.3 Millimeter |