Pure Global

COCHLEAR Nucleus Sound Processor - Indonesia BPOM Medical Device Registration

COCHLEAR Nucleus Sound Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702310173. The device is manufactured by COCHLEAR LIMITED, LANE COVE from Australia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
COCHLEAR Nucleus Sound Processor
Analysis ID: AKL 10702310173

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Australia

Authorized Representative

PT. KASOEM HEARING

AR Address

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

Registration Date

Mar 08, 2024

Expiry Date

Nov 07, 2028

Product Type

Prosthetic Ear, Nose and Throat Equipment

(Deleted) Hearing Aid.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name