CLAMP FORCEPS

GUDID 00192896101081

PUTTERMAN CLAMP FORCEPS WITH INSIDE SCREW LOCK CROSS ACTION T-SHAPED TIP

SONTEC INSTRUMENTS, INC.

Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Primary Device ID00192896101081
NIH Device Record Key018d2e47-7402-49c9-838c-5724b6d2e83a
Commercial Distribution StatusIn Commercial Distribution
Brand NameCLAMP FORCEPS
Version Model Number14-9420
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 Identifiers

Device Issuing AgencyDevice ID
GS100192896101081 [Primary]

FDA Product Code

HNRForceps, ophthalmic
HOBClamp, Muscle, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101081]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-24
Device Publish Date2020-03-16

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