LODE Valiant II Rehab - Indonesia BPOM Medical Device Registration
LODE Valiant II Rehab is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403718294. 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 TRIPATRIA MAINSTAY MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LODE B.V.Country of Origin
Netherlands
Authorized Representative
TRIPATRIA MAINSTAY MEDIKAAR Address
Jl Musi No. 37 Jakarta 10150
Registration Date
Aug 21, 2021
Expiry Date
Sep 01, 2025
Product Type
Therapeutic Physical Health Equipment
Measuring exercise equipment.
Non Radiation Electromedics
LODE Angio Imaging - with Stress Support Radiology
LODE Cardiac Rehab Manager (LCRM)
COST MED Cost ER2100 Treadmil
LODE Ergometers Corival
LODE Angio with Echo Cardiac Stress Table
LODE Corival Pediatric
LODE Corival Recumbent
LODE Corival Rehab
LODE Treadmill Valiant 2 CPET
COMPEX WIRELESS MUSCLE STIMULATOR
DOMEX TECHNOLOGY CORPORATION
COSMED Q-NRG+
COSMED S.R.L
COSMED Quark RMR
COSMED S.R.L.
COSMED Q-BOX Body Plethysmography
COSMED S.R.L.
COSMED Quark PFT
COSMED S.R.L.
COSMED Quark CPET
COSMED S.R.L.
LODE Angio Imaging - with Stress Support Radiology
LODE B.V.
LODE Cardiac Rehab Manager (LCRM)
LODE B.V.
AFIAS IL-6
BODITECH WITH INC.
AFIAS EAA
BODITECH WITH INC