TIMEWAVER - Indonesia BPOM Medical Device Registration
TIMEWAVER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003121120. The device is manufactured by TIMEWAVER PRODUCTION GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TIMEWAVER PRODUCTION GMBHCountry of Origin
Germany
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Mar 03, 2021
Expiry Date
Mar 10, 2025
Product Type
Therapeutic Neurology Equipment
Transcutaneous electrical nerve stimulator for pain relief.
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