DOCTOR LIFE Intermittent Pneumatic Compression System - Indonesia BPOM Medical Device Registration
DOCTOR LIFE Intermittent Pneumatic Compression System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505320297. The device is manufactured by DAESUNG MAREF CO.,LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is KMD INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DAESUNG MAREF CO.,LTD.Country of Origin
Korea
Authorized Representative
KMD INDONESIAAR Address
Menara PALMA lantai 7-06 B, Jl. HR. Rasuna Said
Registration Date
Nov 06, 2023
Expiry Date
Nov 02, 2027
Product Type
Therapeutic Cardiology Equipment
Compressible limb sleeve.
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