BONE TAMP

GUDID 00192896101524

BONE TAMP

SONTEC INSTRUMENTS, INC.

Bone tap, reusable Bone tap, reusable
Primary Device ID00192896101524
NIH Device Record Key26e1bf96-b647-4791-8edf-6deaaefc3cf9
Commercial Distribution StatusIn Commercial Distribution
Brand NameBONE TAMP
Version Model Number1103-197A
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

Device Dimensions

Length8 Inch
Device Size Text, specify0
Length8 Inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896101524 [Primary]
GS100192896101524 [Primary]

FDA Product Code

HWXTAP, BONE
HWXTAP, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896101524]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896101524]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-19
Device Publish Date2020-05-11

On-Brand Devices [BONE TAMP]

00192896082731BONE TAMP BAYONET TIP
00192896052130BONE TAMP
00192896052123BONE TAMP
00192896101524BONE TAMP

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.