BONE HOOK 320-936

GUDID 00192896029286

BONE HOOK SHARP TIP PHENOLIC T HANDLE

SONTEC INSTRUMENTS, INC.

Bone hook
Primary Device ID00192896029286
NIH Device Record Key4b26360e-d5da-4779-b63d-738d8971419f
Commercial Distribution StatusIn Commercial Distribution
Brand NameBONE HOOK
Version Model Number320-936
Catalog Number320-936
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896029286 [Primary]

FDA Product Code

KIKHOOK, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896029286]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-15
Device Publish Date2018-09-13

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