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LINA-SURGIPEN™ ELECTROSURGICAL HANDSWITCH PENCIL - FDA Registration DVR-7368

Access comprehensive regulatory information for LINA-SURGIPEN™ ELECTROSURGICAL HANDSWITCH PENCIL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-7368 and manufactured by LiNA Medical ApS - Formervangen 5, 2600 Glostrup Denmark mfd. by: LiNA Medical Polska SP. z.o.o - UL Rolna 8A, Sady 62-080 Tarnowo Podgorne Poland in Poland. The device was registered on October 31, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Patient Care Corporation), 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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Poland
DVR-7368
LINA-SURGIPEN™ ELECTROSURGICAL HANDSWITCH PENCIL
Registered medical device in Philippines
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Device Information
Product Name
LINA-SURGIPEN™ ELECTROSURGICAL HANDSWITCH PENCIL
Registration Number
DVR-7368
Importer & Distribution
Importer/Distributor
Patient Care Corporation
Registration Dates
Issuance Date
October 31, 2024
Expiry Date
June 11, 2029