UROLOGICAL GYNECOLOGICAL RETRACTOR 520-250

GUDID 00192896045811

UROLOGICAL GYNECOLOGICAL RETRACTOR SLING SPACER ANGLED SHAFT

SONTEC INSTRUMENTS, INC.

Surgical retractor/retraction system blade, reusable
Primary Device ID00192896045811
NIH Device Record Key6b8af606-18b4-467d-bcf6-f1a17e7edfb5
Commercial Distribution StatusIn Commercial Distribution
Brand NameUROLOGICAL GYNECOLOGICAL RETRACTOR
Version Model Number520-250
Catalog Number520-250
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100192896045811 [Primary]

FDA Product Code

HDLRETRACTOR, VAGINAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896045811]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-03-11
Device Publish Date2018-10-04

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