Collin-Duval Intestinal Clamp 2200-603

GUDID 00192896120136

Collin-Duval Intestinal Clamp Serrated

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID00192896120136
NIH Device Record Key5f26d7bf-bdee-4a90-bdb4-f84125172569
Commercial Distribution StatusIn Commercial Distribution
Brand NameCollin-Duval Intestinal Clamp
Version Model Number2200-603
Catalog Number2200-603
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
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch
Length9 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896120136 [Primary]

FDA Product Code

HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


[00192896120136]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-21
Device Publish Date2024-10-11

On-Brand Devices [Collin-Duval Intestinal Clamp]

00192896100503COLLIN-DUVAL INTESTINAL CLAMP SERRATED
00192896120136Collin-Duval Intestinal Clamp Serrated

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