ENDOMED 682V - Indonesia BPOM Medical Device Registration
ENDOMED 682V is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003904368. The device is manufactured by ENRAF NONIUS B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ENRAF NONIUS B.V.Country of Origin
Netherlands
Authorized Representative
PT. MURTI INDAH SENTOSAAR Address
WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH
Registration Date
Apr 22, 2019
Expiry Date
Nov 28, 2023
Product Type
Therapeutic Neurology Equipment
Transcutaneous electrical nerve stimulator for pain relief.
Non Radiation Electromedics
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