JOIMAX Shrill System - Indonesia BPOM Medical Device Registration
JOIMAX Shrill System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21303220197. The device is manufactured by JOIMAX GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTEK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JOIMAX GMBHCountry of Origin
Germany
Authorized Representative
PT. MEDTEKAR Address
DELTA BUILDING BLOK A-11, C-1 & C-2, JL. SURYOPRANOTO NO.1-9, RT/RW 004/007
Registration Date
Jun 24, 2024
Expiry Date
Dec 31, 2025
Product Type
Surgical Orthopaedic Equipment
Sonic surgical instrument and accessories/attachments.
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