ARTHROSCOPIC TENDON KNIFE 1271-131

GUDID 00192896084018

ARTHROSCOPIC TENDON KNIFE ROUND KNURL HANDLE

SONTEC INSTRUMENTS, INC.

Bone lever/elevator Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable Bone lever/elevator, reusable
Primary Device ID00192896084018
NIH Device Record Key7763d449-8925-457f-b2cd-271b46185227
Commercial Distribution StatusIn Commercial Distribution
Brand NameARTHROSCOPIC TENDON KNIFE
Version Model Number1271-131
Catalog Number1271-131
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
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896084018 [Primary]

FDA Product Code

HTSKNIFE, ORTHOPEDIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896084018]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-04
Device Publish Date2018-09-21

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