Philippines FDA registration MDR-10718

POLYMED SAFETY SCALP VEIN SET SAFETY WINGED INFUSION SET

Philippines·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·India·Issued August 06, 2024 – December 29, 2026

Device information

Product Name: POLYMED SAFETY SCALP VEIN SET SAFETY WINGED INFUSION SET
Registration Number: MDR-10718

Manufacturer details

Manufacturer: 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
Country of Origin: India

Importer & distribution

Importer/Distributor: Iraseth Pharma Inc.

Registration dates

Issuance Date: August 06, 2024
Expiry Date: December 29, 2026

About this record

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.