Primary Device ID | 00192896110144 |
NIH Device Record Key | 224cc634-6737-4173-a89f-1787e3f336dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kitzmiller Forceps |
Version Model Number | 2600-100R |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Length | 5.5 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896110144 [Primary] |
DWS | INSTRUMENTS, SURGICAL, CARDIOVASCULAR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896110144]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-06-09 |
Device Publish Date | 2021-06-01 |
00192896098121 | KITZMILLER FORCEPS RIGHT HANDED TITANIUM |
00192896098114 | KITZMILLER FORCEPS LEFT HANDED TITANIUM |
00192896110144 | Kitzmiller Forceps Cooley Jaws Angled Right Titanium |
00192896110137 | Kitzmiller Forceps Cooley Jaws Angled Left Titanium |