BAIRD CHALAZION FORCEPS T14-9850

GUDID 00192896090149

BAIRD CHALAZION FORCEPS SMALL OVAL TIPS TITANIUM

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 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 ID00192896090149
NIH Device Record Key2ff8ebca-7ec4-4363-bcc1-a2f9b439aa9d
Commercial Distribution StatusIn Commercial Distribution
Brand NameBAIRD CHALAZION FORCEPS
Version Model NumberT14-9850
Catalog NumberT14-9850
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 Latexfalse
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
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
GS100192896090149 [Primary]

FDA Product Code

HNRForceps, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896090149]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-07-12
Device Publish Date2018-10-24

On-Brand Devices [BAIRD CHALAZION FORCEPS]

00192896090149BAIRD CHALAZION FORCEPS SMALL OVAL TIPS TITANIUM
00192896017252BAIRD CHALAZION FORCEPS SMALL OVAL TIP

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