CAPSULUS - Indonesia BPOM Medical Device Registration
CAPSULUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203220068. The device is manufactured by OPTOTEK D.O.O. from Slovakia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SURYA TAMA MEDIKA.
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CAPSULO
Risk Classification
Product Class
Kelas : 2
Manufacturer
OPTOTEK D.O.O.Country of Origin
Slovakia
Authorized Representative
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
Jan 17, 2024
Expiry Date
Jan 17, 2029
Product Type
Surgical Eye Equipment
Ophthalmic laser.
Non Radiation Electromedics
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