CASTROVIEJO CYCLODIALYSIS SPATULA T12-3500

GUDID 00192896072770

CASTROVIEJO CYCLODIALYSIS SPATULA DOUBLE ENDED WIDE BLUNT BLADES 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 ID: 00192896072770
• NIH Device Record Key: 4cb3ad83-5372-433e-aae5-8387331e1fa9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CASTROVIEJO CYCLODIALYSIS SPATULA
• Version Model Number: T12-3500
• Catalog Number: T12-3500
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896072770 [Primary]

FDA Product Code

• HND: Spatula, ophthalmic

Sterilization

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

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072770]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-02-24
• Device Publish Date: 2018-09-19

On-Brand Devices [CASTROVIEJO CYCLODIALYSIS SPATULA]

• 00192896072770: CASTROVIEJO CYCLODIALYSIS SPATULA DOUBLE ENDED WIDE BLUNT BLADES TITANIUM
• 00192896013445: CASTROVIEJO CYCLODIALYSIS SPATULA DOUBLE ENDED WIDE BLUNT TIPS STAINLESS STEEL
• 00192896013438: CASTROVIEJO CYCLODIALYSIS SPATULA DOUBLE ENDED WIDE BLUNT TIPS STAINLESS STEEL