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EMOS Flexible Bronchoscope - Indonesia BPOM Medical Device Registration

EMOS Flexible Bronchoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703120767. The device is manufactured by EMOS TECHNOLOGY GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIADI LINTAS PERSADA.

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
EMOS Flexible Bronchoscope
Analysis ID: AKL 20703120767

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. TRIADI LINTAS PERSADA

AR Address

Ruko Exclusive Raden Inten Jl. Raden Inten II No. 80 Kav. 5

Registration Date

May 16, 2023

Expiry Date

Apr 01, 2026

Product Type

Ear, Nose and Throat Surgical Equipment

Bronchoscope (flexible or rigid) and accessories.

Non Electromedic Non Sterile

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