PIN PULLING PLIERS 1100-533

GUDID 00192896048027

PIN PULLING PLIERS DOUBLE ACTON TUNGSTEN CARBIDE SERRATED TIP

SONTEC INSTRUMENTS, INC.

Orthopaedic joint/limb rongeur
Primary Device ID00192896048027
NIH Device Record Key437363b1-0aac-4ac6-b895-9c0096b97e0e
Commercial Distribution StatusIn Commercial Distribution
Brand NamePIN PULLING PLIERS
Version Model Number1100-533
Catalog Number1100-533
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length7 Inch
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896048027 [Primary]

FDA Product Code

EJYPliers, operative
HWBExtractor

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896048027]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-07-12
Device Publish Date2018-09-12

On-Brand Devices [PIN PULLING PLIERS]

00192896053922PIN PULLING PLIERS TUNGSTEN CARBIDE TIP
00192896048027PIN PULLING PLIERS DOUBLE ACTON TUNGSTEN CARBIDE SERRATED TIP
00192896048010PIN PULLING PLIERS DOUBLE ACTION TUNGSTEN CARBIDE SERRATED TIP
00192896111615Pin Pulling Pliers Double Action Tungsten Carbide Serrated

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.