BEURER Nebuliser - Indonesia BPOM Medical Device Registration
BEURER Nebuliser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403312710. The device is manufactured by BEURER GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEURER GMBH.Country of Origin
Germany
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Jul 25, 2022
Expiry Date
Oct 19, 2025
Product Type
Therapeutic Anesthesia Equipment
Nebulizer.
Non Radiation Electromedics
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