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Cochlear™ Baha 6 Max Sound Processor - Indonesia BPOM Medical Device Registration

Cochlear™ Baha 6 Max Sound Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702123556. The device is manufactured by COCHLEAR BONE ANCHORED SOLUTION AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is KASOEM HEARING.

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.

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BPOM Registered
Risk Class Kelas Resiko : B
Cochlear™ Baha 6 Max Sound Processor
Analysis ID: AKL 20702123556

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

KASOEM HEARING

AR Address

Jl. Setiabudi No. 34, RT 002 RW 003, Kel. Hegarmanah, Kec. Cidadap, Kota Bandung, Jawa Barat

Registration Date

Jul 29, 2024

Expiry Date

Jun 14, 2029

Product Type

Prosthetic Ear, Nose and Throat Equipment

Wireless air-conduction hearing aid

Non Radiation Electromedics

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