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Bausch + Lomb Bipolar Eraser (with Lemo-type Connector) - FDA Registration CMDR-2023-02039A

Access comprehensive regulatory information for Bausch + Lomb Bipolar Eraser (with Lemo-type Connector) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-02039A and manufactured by Bausch & Lomb GmbH Im Schuhmachergewann 4, 69123 Heidelberg, Germany in Germany. The device was registered on October 20, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Bausch and Lomb Philippines, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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Germany
CMDR-2023-02039A
Bausch + Lomb Bipolar Eraser (with Lemo-type Connector)
Registered medical device in Philippines
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Device Information
Product Name
Bausch + Lomb Bipolar Eraser (with Lemo-type Connector)
Registration Number
CMDR-2023-02039A
Manufacturer Details
Importer & Distribution
Registration Dates
Issuance Date
October 20, 2023
Expiry Date
October 20, 2028