Medium Blade Pair for Debakey Retractor 2500-552

GUDID 00192896121119

Medium Blade Pair for Debakey Retractor Child Size

SONTEC INSTRUMENTS, INC.

Surgical retractor/retraction system blade, reusable
Primary Device ID00192896121119
NIH Device Record Key32533ed7-c542-4152-ab0e-6a32db96c595
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedium Blade Pair for Debakey Retractor
Version Model Number2500-552
Catalog Number2500-552
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896121119 [Primary]

FDA Product Code

GADRETRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

[00192896121119]

Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-14
Device Publish Date2025-02-06

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