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VieCare Extracorporeal Shock Wave Lithotripter - Indonesia BPOM Medical Device Registration

VieCare Extracorporeal Shock Wave Lithotripter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420527. The device is manufactured by SHENZHEN HYDE MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GAMAMED.

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 : C
VieCare Extracorporeal Shock Wave Lithotripter
Analysis ID: AKL 20805420527

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GAMAMED

AR Address

JL. WR. SUPRATMAN 56 B

Registration Date

Oct 18, 2024

Expiry Date

Oct 16, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Extracorporeal shock wave lithotripter.

Non Radiation Electromedics

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