TECHNOLAS® TENEO™ 317 - Indonesia BPOM Medical Device Registration
TECHNOLAS® TENEO™ 317 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203916107. The device is manufactured by TECHNOLAS PERFECT VISION GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GLOBAL ALIGNED MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TECHNOLAS PERFECT VISION GMBHCountry of Origin
Germany
Authorized Representative
GLOBAL ALIGNED MEDIKAAR Address
RUKO PULOGADUNG TRADE CENTRE (PTC) BLOK 8-A NO.7 JL.RAYA BEKASI KM.21 RT.003 RW.003 RAWA TERATE,CAKUNG,JAKARTA TIMUR
Registration Date
Jul 26, 2023
Expiry Date
Jun 07, 2028
Product Type
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