FAROMED Head Light - Indonesia BPOM Medical Device Registration
FAROMED Head Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203021379. The device is manufactured by FAROMED GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FA ANTARES MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FAROMED GMBHCountry of Origin
Germany
Authorized Representative
FA ANTARES MEDIKAAR Address
RUKO GOLDEN BOULEVARD BLOK I NO.7
Registration Date
Nov 23, 2023
Expiry Date
Nov 14, 2028
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
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