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TENDRIL MRI™ ACTIVE FIXATION BIPOLAR STEROID-ELUTING ENDOCARDIAL PACING LEAD - FDA Registration MDR-01834

Access comprehensive regulatory information for TENDRIL MRI™ ACTIVE FIXATION BIPOLAR STEROID-ELUTING ENDOCARDIAL PACING LEAD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01834 and manufactured by Abbott Medical (Singapore) Pte. Ltd. in USA. The device was registered on March 25, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Biodevices 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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MDR-01834
TENDRIL MRI™ ACTIVE FIXATION BIPOLAR STEROID-ELUTING ENDOCARDIAL PACING LEAD
Registered medical device in Philippines
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Device Information
Product Name
TENDRIL MRI™ ACTIVE FIXATION BIPOLAR STEROID-ELUTING ENDOCARDIAL PACING LEAD
Registration Number
MDR-01834
Manufacturer Details
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Biodevices Inc.
Registration Dates
Issuance Date
March 25, 2020
Expiry Date
February 25, 2025