SONTEC 5D ARCULATE MARKER T12-8502

GUDID 00192896097100

SONTEC 5D ARCULATE MARKER WITH ALIGNMENT NOTCHES ROUND HANDLE TITANIUM

SONTEC INSTRUMENTS, INC.

Corneal marker, reusable

• Primary Device ID: 00192896097100
• NIH Device Record Key: 14d0eeff-4364-425c-908c-11d106defdc1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONTEC 5D ARCULATE MARKER
• Version Model Number: T12-8502
• Catalog Number: T12-8502
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 4 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896097100 [Primary]

FDA Product Code

• HMQ: Marker, Sclera

Sterilization

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

[00192896097100]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-17
• Device Publish Date: 2019-05-09

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