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SERENITY Turnstile - Indonesia BPOM Medical Device Registration

SERENITY Turnstile is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11604320040. The device is manufactured by ZHEJIANG HONSUN MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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.

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BPOM Registered
Risk Class Kelas Resiko : A
SERENITY Turnstile

SERENITY Tourniquet

Analysis ID: AKL 11604320040

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SERENITY INDONESIA

AR Address

Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01

Registration Date

Oct 04, 2023

Expiry Date

Aug 07, 2028

Product Type

Therapeutic Surgical Equipment

Nonpneumatic tourniquet.

Non Electromedic Non Sterile

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