POTTS COOLEY TISSUE FORCEPS 2205-655

GUDID 00192896092969

POTTS COOLEY TISSUE FORCEPS EXTRA SERRATED TIP

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID00192896092969
NIH Device Record Keycbdad8a9-68b0-4aab-ad8e-fee1c73f2675
Commercial Distribution StatusIn Commercial Distribution
Brand NamePOTTS COOLEY TISSUE FORCEPS
Version Model Number2205-655
Catalog Number2205-655
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

Device Dimensions

Length9.5 Inch
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896092969 [Primary]

FDA Product Code

HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896092969]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-08-21
Device Publish Date2019-01-03

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