Iris Forceps

GUDID 00192896102613

Gill Iris Tissue Forceps Colibri Style Curved Tip 1x2 Box Teeth

SONTEC INSTRUMENTS, INC.

Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Primary Device ID00192896102613
NIH Device Record Keybf7ae28a-9dfd-4c8e-8203-69188407b2ef
Commercial Distribution StatusIn Commercial Distribution
Brand NameIris Forceps
Version Model Number14-1310
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

Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch
Length6.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]
GS100192896102613 [Primary]

FDA Product Code

HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic
HNRForceps, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102613]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-23
Device Publish Date2020-06-15

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