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LUMINA Flexible Videoscopes Reusable - Indonesia BPOM Medical Device Registration

LUMINA Flexible Videoscopes Reusable is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403520024. The device is manufactured by ZHEJIANG UE MEDICAL CORP. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PROCARE MEDITECH LIGHT.

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
LUMINA Flexible Videoscopes Reusable
Analysis ID: AKL 20403520024

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PROCARE MEDITECH LIGHT

AR Address

Jl. Jakarta Garden City, Ruko New East Blok. NE, No.39

Registration Date

Jan 15, 2025

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Anesthesia Equipment

Flexible laryngoscope.

Non Radiation Electromedics

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