LODE Corival Rehab - Indonesia BPOM Medical Device Registration
LODE Corival Rehab is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403718208. The device is manufactured by LODE B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIPATRIA MAINSTAY MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LODE B.V.Country of Origin
Netherlands
Authorized Representative
PT. TRIPATRIA MAINSTAY MEDIKAAR Address
Jl Musi No. 37 Jakarta 10150
Registration Date
Aug 17, 2021
Expiry Date
Sep 01, 2025
Product Type
Therapeutic Physical Health Equipment
Measuring exercise equipment.
Non Radiation Electromedics
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