MICASEPT DEBAKEY PERIPHERAL CLAMP 20919-08-037

GUDID 00192896008311

MICASEPT DEBAKEY PERIPHERAL CLAMP WITH HEGAR RATCHET LONG JAW

SONTEC INSTRUMENTS, INC.

Rigid endoscopic grasping forceps, reusable
Primary Device ID00192896008311
NIH Device Record Key8c25a3b0-ad01-4849-b803-ffc50361a457
Commercial Distribution StatusIn Commercial Distribution
Brand NameMICASEPT DEBAKEY PERIPHERAL CLAMP
Version Model Number20919-08-037
Catalog Number20919-08-037
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Phone800-821-7496
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 Dimensions

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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896008311 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896008311]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-17
Device Publish Date2018-08-15

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