LYMPHATOUCH LT01 - Indonesia BPOM Medical Device Registration
LYMPHATOUCH LT01 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403913649. The device is manufactured by LYMPHATOUCH INC. from Finland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LYMPHATOUCH INC.Country of Origin
Finland
Authorized Representative
PT. MURTI INDAH SENTOSAAR Address
WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH
Registration Date
May 10, 2023
Expiry Date
Dec 31, 2028
Product Type
Therapeutic Physical Health Equipment
Presssure-applying device.
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