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HUAN KANG Stomach Tube - Indonesia BPOM Medical Device Registration

HUAN KANG Stomach Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220128. The device is manufactured by CHANGZHOU HUANKANG MEDICAL DEVICE CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALEXA MEDIKA.

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 : B
HUAN KANG Stomach Tube
Analysis ID: AKL 20805220128

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ALEXA MEDIKA

AR Address

Jl. Yos Sudarso Komplek Graha Niaga Blok C No. 14

Registration Date

May 12, 2022

Expiry Date

Jan 21, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Gastrointestinal tube and accessories.

Non Electromedic Sterile

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