PHONAK TERRA+ BTE-M - Indonesia BPOM Medical Device Registration
PHONAK TERRA+ BTE-M is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702520010. The device is manufactured by SONOVA AT from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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
SONOVA ATCountry of Origin
Switzerland
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Jan 17, 2025
Expiry Date
Nov 30, 2028
Product Type
Prosthetic Ear, Nose and Throat Equipment
Wireless air-conduction hearing aid
Non Radiation Electromedics
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PHONAK TERRA+ RIC-312
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PHONAK TERRA BTE-M
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PHONAK TERRA+ BTE-UP
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