AVIAN SET 1103-900-SET

GUDID 00192896053748

AVIAN SET WITH TRAY TITANIUM

SONTEC INSTRUMENTS, INC.

General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable General surgical procedure kit, non-medicated, reusable
Primary Device ID00192896053748
NIH Device Record Key93a85040-c2e2-465e-aaaa-c9ee089e0e61
Commercial Distribution StatusIn Commercial Distribution
Brand NameAVIAN SET
Version Model Number1103-900-SET
Catalog Number1103-900-SET
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
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896053748 [Primary]

FDA Product Code

GZXINSTRUMENT, MICROSURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896053748]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-05-03
Device Publish Date2018-09-24

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