ROSSMAX Stethoscope - Indonesia BPOM Medical Device Registration
ROSSMAX Stethoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10401713799. The device is manufactured by ROSSMAX (SHANGHAI) INCORPORATION LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDISINDO BAHANA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ROSSMAX (SHANGHAI) INCORPORATION LTD.Country of Origin
China
Authorized Representative
PT. MEDISINDO BAHANAAR Address
Rukan Graha Cempaka Mas Blok E No.15 Lt.3, Jl. Letjen Suprapto No.1, Jakarta Pusat
Registration Date
Apr 05, 2021
Expiry Date
Feb 21, 2025
Product Type
Diagnostic Anesthesia Equipment
Stethoscope head.
Non Electromedic Non Sterile
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