LASIK FLAP SPATULA T12-2860

GUDID 00192896013384

LASIK FLAP SPATULA SINGLE ENDED BLADE TITANIUM

SONTEC INSTRUMENTS, INC.

Ocular hook/spatula/manipulator, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable Ophthalmic surgical probe, reusable
Primary Device ID00192896013384
NIH Device Record Keyd0d59bdf-fff4-40c0-bfa6-da23ebf08e2d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLASIK FLAP SPATULA
Version Model NumberT12-2860
Catalog NumberT12-2860
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

Device Dimensions

Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter
Width2 Millimeter
Length11.8 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896013384 [Primary]

FDA Product Code

HNDSpatula, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896013384]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2018-09-18

On-Brand Devices [LASIK FLAP SPATULA]

00192896072749LASIK FLAP SPATULA SINGLE ENDED BLADE
00192896013384LASIK FLAP SPATULA SINGLE ENDED BLADE TITANIUM

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