INION FixOn ™ Titanium Suture Anchor - Indonesia BPOM Medical Device Registration
INION FixOn ™ Titanium Suture Anchor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302022357. The device is manufactured by INION LTD from Finland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EUPHRATES WITH.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
INION LTDCountry of Origin
Finland
Authorized Representative
PT. EUPHRATES WITHAR Address
Ruko Gardenia kav 1, jln. parigi raya no 75 sukabakti curug 15810
Registration Date
Apr 25, 2020
Expiry Date
Sep 04, 2024
Product Type
Prosthetic Orthopedic Equipment
Single/multiple component metallic bone fixation appliances and accessories.
Non Electromedic Sterile
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INION FixOn ™ Biocomposite Suture Anchor
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