Pure Global

HEINE Mini 3000 F.O. Otoscope - Indonesia BPOM Medical Device Registration

HEINE Mini 3000 F.O. Otoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703127936. The device is manufactured by HEINE OPTOTECHNIK GMBH & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is LABORA MANDIRI INDO PRATAMA.

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
HEINE Mini 3000 F.O. Otoscope
Analysis ID: AKL 10703127936

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47, RT.014, RW.003, Desa/Kelurahan Terban, Kecamanan Gondokusuman, Kota Yogyakarta, Provinsi Daerah Istimewa Yogyakarta, Kode Pos : 55223

Registration Date

Jun 10, 2024

Expiry Date

Dec 31, 2027

Product Type

Ear, Nose and Throat Surgical Equipment

Otoscope.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing