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Telescope Ultra - FDA Registration 2b101b4a3729a0d668ed370dde472a93

Access comprehensive regulatory information for Telescope Ultra in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2b101b4a3729a0d668ed370dde472a93 and manufactured by Olympus Winter & Ibe GmbH. The device was registered on October 29, 2021.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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2b101b4a3729a0d668ed370dde472a93
Telescope Ultra
FDA ID: 2b101b4a3729a0d668ed370dde472a93
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Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
2b101b4a3729a0d668ed370dde472a93
Registration Date
October 29, 2021
Authorized Representative