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SERENITY Spine Board - Indonesia BPOM Medical Device Registration

SERENITY Spine Board is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903411243. The device is manufactured by ZHANGJIAGANG NEW FELLOW MED., 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 Spine Board
Analysis ID: AKL 10903411243

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SERENITY INDONESIA

AR Address

Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter

Registration Date

Feb 27, 2023

Expiry Date

Feb 07, 2028

Product Type

General Hospital Equipment and Other Individuals

Hand-carried stretcher.

Non Electromedic Non Sterile

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