LASIK FLAP SPATULA 12-2860

GUDID 00192896072749

LASIK FLAP SPATULA SINGLE ENDED BLADE

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 ID: 00192896072749
• NIH Device Record Key: c4815394-71be-4b21-a8e0-b704dba6743f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LASIK FLAP SPATULA
• Version Model Number: 12-2860
• Catalog Number: 12-2860
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter
• Width: 2 Millimeter
• Length: 11.8 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896072749 [Primary]

FDA Product Code

• HND: Spatula, ophthalmic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896072749]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2018-09-19

On-Brand Devices [LASIK FLAP SPATULA]

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