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POLYMED SAFETY SCALP VEIN SET SAFETY WINGED INFUSION SET - FDA Registration MDR-10718

Access comprehensive regulatory information for POLYMED SAFETY SCALP VEIN SET SAFETY WINGED INFUSION SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10718 and manufactured by Poly Medicure Limited -232-B, 3rd Floor, Okhla Industrial Estate, Phase III, New Delhi-110020 India. Mfd by: Poly Medicure Limited - Plot No. 104-109, Sector - 59, HSIIDC Indl. Area, Ballabhgarh, Faridabad - 121004, (Haryana), India in India. The device was registered on August 06, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Iraseth Pharma 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-10718
POLYMED SAFETY SCALP VEIN SET SAFETY WINGED INFUSION SET
Registered medical device in Philippines
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Device Information
Product Name
POLYMED SAFETY SCALP VEIN SET SAFETY WINGED INFUSION SET
Registration Number
MDR-10718
Importer & Distribution
Importer/Distributor
Iraseth Pharma Inc.
Registration Dates
Issuance Date
August 06, 2024
Expiry Date
December 29, 2026