FEMORAL HEAD DISARTICULATOR KNIFE 1103-213

GUDID 00192896090033

FEMORAL HEAD DISARTICULATOR KNIFE LARGE SIZE CURVED BLADE

SONTEC INSTRUMENTS, INC.

Meniscus knife
Primary Device ID00192896090033
NIH Device Record Keyf8268a4d-ef36-490b-81ab-a11012a7049a
Commercial Distribution StatusIn Commercial Distribution
Brand NameFEMORAL HEAD DISARTICULATOR KNIFE
Version Model Number1103-213
Catalog Number1103-213
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

Length7.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896090033 [Primary]

FDA Product Code

HTSKNIFE, ORTHOPEDIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896090033]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-06-10
Device Publish Date2018-10-24

On-Brand Devices [FEMORAL HEAD DISARTICULATOR KNIFE]

00192896090040FEMORAL HEAD DISARTICULATOR KNIFE SMALL SIZE CURVED BLADE
00192896090033FEMORAL HEAD DISARTICULATOR KNIFE LARGE SIZE CURVED BLADE
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