Arthroscopic Bayonet Knife 1271-119T

GUDID 00192896121560

Arthroscopic Bayonet Knife Triangle Handle

SONTEC INSTRUMENTS, INC.

Orthopaedic knife
Primary Device ID00192896121560
NIH Device Record Keyb0c4d64a-c934-4913-839d-ac0cbf148514
Commercial Distribution StatusIn Commercial Distribution
Brand NameArthroscopic Bayonet Knife
Version Model Number1271-119T
Catalog Number1271-119T
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 Latextrue
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

Device Dimensions

Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896121560 [Primary]

FDA Product Code

HTSKNIFE, ORTHOPEDIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896121560]

Dry Heat Sterilization


[00192896121560]

Dry Heat Sterilization


[00192896121560]

Dry Heat Sterilization


[00192896121560]

Dry Heat Sterilization


[00192896121560]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-22
Device Publish Date2025-05-14

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