OCTAX NAVILASE - Indonesia BPOM Medical Device Registration
OCTAX NAVILASE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105917828. The device is manufactured by VITROLIFE GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NEW MODULE INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VITROLIFE GMBHCountry of Origin
Germany
Authorized Representative
PT. NEW MODULE INTERNATIONALAR Address
Jalan Abdul Muis No. 36 Q Jakarta 10160
Registration Date
Nov 08, 2021
Expiry Date
Oct 31, 2024
Product Type
Reproductive Aids
Assisted reproduction laser system.
Non Radiation Electromedics
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