MK-T105

GUDID 30810003220159

MICROKERATOME Tubing Set. Disposable and have proper keratome fittings with a moisture trap. A precision filter captures the mositure before it can cause damage to your microkeratome console. Sterile. Gebauer Tubing, 5/box.

MICROSPECIALITIES, INC.

Disposable vacuum tubing

• Primary Device ID: 30810003220159
• NIH Device Record Key: 16b36344-8459-46d5-b8cd-6d8479c38ca8
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: MK-T105
• Catalog Number: MK-T105
• Company DUNS: 013469890
• Company Name: MICROSPECIALITIES, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx
• Phone: 203-874-1832
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10810003220155 [Primary]
GS1	30810003220159 [Package]; Contains: 10810003220155; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• GAZ: Tubing, Noninvasive

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-07-04
• Device Publish Date: 2018-10-30

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