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PROVITA Mobile LED Examination Lamp Series 2 - Indonesia BPOM Medical Device Registration

PROVITA Mobile LED Examination Lamp Series 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903812929. The device is manufactured by PROVITA MEDICAL GMBH & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEGA PRATAMA MEDICALINDO.

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 : A
PROVITA Mobile LED Examination Lamp Series 2
Analysis ID: AKL 10903812929

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Sep 24, 2020

Expiry Date

May 23, 2024

Product Type

General Hospital Equipment and Other Individuals

AC-powered medical examination light.

Non Radiation Electromedics

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