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Q-MED LEAD APRON PDW - Indonesia BPOM Medical Device Registration

Q-MED LEAD APRON PDW is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11503027633. The device is manufactured by SHANGDONG DOUBLE EAGLE MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SRI INTAN PERKASA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
Q-MED LEAD APRON PDW
Analysis ID: AKL 11503027633

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SRI INTAN PERKASA

AR Address

RUKO HARAPAN INDAH BLOK EN/7 KOMPLEK HARAPAN INDAH BEKASI BARAT, KOTA BEKASI, JAWA BARAT

Registration Date

Dec 05, 2023

Expiry Date

Dec 04, 2026

Product Type

Other Radiology Equipment

Personnel protective shield.

Non Electromedic Non Sterile

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