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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
ZHANGJIAGANG NEW FELLOW MED., CO., LTD.Country of Origin
China
Authorized Representative
SERENITY INDONESIAAR 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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