THUNDERBEAT Type S - Indonesia BPOM Medical Device Registration
THUNDERBEAT Type S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222348. The device is manufactured by AOMORI OLYMPUS CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AOMORI OLYMPUS CO., LTD.Country of Origin
Japan
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Oct 08, 2022
Expiry Date
Mar 31, 2025
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
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