MICTEC DIRONDAL NEEDLE HOLDER 20918-07-301

GUDID 00192896011373

MICTEC DIRONDAL NEEDLE HOLDER WITH HEGAR RATCHET STRAIGHT TIP SHORT WIDE JAW

SONTEC INSTRUMENTS, INC.

Needle holder, reusable
Primary Device ID00192896011373
NIH Device Record Keyc3dcc2c6-37c7-4d21-9826-949ad50b24f4
Commercial Distribution StatusIn Commercial Distribution
Brand NameMICTEC DIRONDAL NEEDLE HOLDER
Version Model Number20918-07-301
Catalog Number20918-07-301
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
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch
Length11 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896011373 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896011373]

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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