Vein Illuminator

GUDID 06926802602805

MEDCAPTAIN MEDICAL TECHNOLOGY CO., LTD.

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• Primary Device ID: 06926802602805
• NIH Device Record Key: 5093a2ef-114c-4cb5-ab79-2b28b8123421
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vein Illuminator
• Version Model Number: NAVI-30
• Company DUNS: 543036737
• Company Name: MEDCAPTAIN MEDICAL TECHNOLOGY CO., LTD.
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com
• Phone: +8675526953369
• Email: mc.service@medcaptain.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06926802602805 [Primary]

FDA Product Code

• KZA: Device, Vein Location, Liquid Crystal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-13
• Device Publish Date: 2024-02-05

On-Brand Devices [Vein Illuminator]

• 06926802602812: NAVI-60
• 06926802602805: NAVI-30