LINDEMANN AMPUTATION SAW 345-214

GUDID 00192896031425

LINDEMANN AMPUTATION SAW

SONTEC INSTRUMENTS, INC.

Manual surgical saw, rigid
Primary Device ID00192896031425
NIH Device Record Key6ba9463d-8c80-41d5-a1a3-2360347ead11
Commercial Distribution StatusIn Commercial Distribution
Brand NameLINDEMANN AMPUTATION SAW
Version Model Number345-214
Catalog Number345-214
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

Length8 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896031425 [Primary]

FDA Product Code

GDRSAW, MANUAL AND ACCESSORIES

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896031425]

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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