GIGLI SAW BLADE 1100-505

GUDID 00192896047914

GIGLI SAW BLADE

SONTEC INSTRUMENTS, INC.

Manual surgical saw, flexible
Primary Device ID00192896047914
NIH Device Record Key733d1467-d863-44ed-aa66-c6490266becb
Commercial Distribution StatusIn Commercial Distribution
Brand NameGIGLI SAW BLADE
Version Model Number1100-505
Catalog Number1100-505
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

Length30 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896047914 [Primary]

FDA Product Code

GDRSAW, MANUAL AND ACCESSORIES

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896047914]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-05-16
Device Publish Date2018-09-14

On-Brand Devices [GIGLI SAW BLADE]

00192896047914GIGLI SAW BLADE
00192896047907GIGLI SAW BLADE
00192896047891GIGLI SAW BLADE

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