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 20505125176. 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.,LTDCountry of Origin
Korea
Authorized Representative
KMD INDONESIAAR Address
Menara Palma lantai 7-06B, Jl. HR. Rasuna Said, Blok X2 Kav. 6 RT 009 RW 004, Kelurahan Kuningan Timur
Registration Date
Mar 01, 2023
Expiry Date
Nov 02, 2027
Product Type
Therapeutic Cardiology Equipment
Compressible limb sleeve.
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