ROOM OptonPro - Indonesia BPOM Medical Device Registration
ROOM OptonPro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403128071. The device is manufactured by ZIMMER MEDIZINSYSTEME GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURYA TAMA MEDIKA.
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ZIMMER OptonPro
Risk Classification
Product Class
Kelas : 2
Manufacturer
ZIMMER MEDIZINSYSTEME GMBH.Country of Origin
Germany
Authorized Representative
PT. SURYA TAMA MEDIKAAR Address
Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi
Registration Date
Dec 20, 2021
Expiry Date
Dec 20, 2026
Product Type
Therapeutic Physical Health Equipment
Ultrasound and muscle stimulator for use in applying therapeutic deep heat for selected medical conditions
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