SERENITY Male External Catheter - Indonesia BPOM Medical Device Registration
SERENITY Male External Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805111155. The device is manufactured by ZHANJIANG STAR ENTERPRISE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
ZHANJIANG STAR ENTERPRISE CO., LTD.Country of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Dec 29, 2020
Expiry Date
Aug 25, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urine collector and accessories
Non Electromedic Sterile
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