SONTEC JORDAN RING RETRACTOR FRAME

GUDID 00192896101586

SONTEC JORDAN RING RETRACTOR FRAME SEGMENTED, SLOTTED

SONTEC INSTRUMENTS, INC.

Laparotomy ring
Primary Device ID00192896101586
NIH Device Record Keybcc9a597-54a1-4c01-9b5d-ed8a414c1b27
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC JORDAN RING RETRACTOR FRAME
Version Model Number516-852
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 Latextrue
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

Device Dimensions

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

Device Issuing AgencyDevice ID
GS100192896101586 [Primary]

FDA Product Code

FFORetractor, Self-Retaining
HXPINSTRUMENT, BENDING OR CONTOURING

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101586]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-19
Device Publish Date2020-05-11

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