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N-Line Pro - Indonesia BPOM Medical Device Registration

N-Line Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420709. The device is manufactured by MEDLIGHT, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AESENDIA INFINI INDONESIA.

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
N-Line Pro
Analysis ID: AKL 21603420709

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDLIGHT, GMBH

Country of Origin

Germany

Authorized Representative

AESENDIA INFINI INDONESIA

AR Address

Business Park Kebon Jeruk Blok D2 No. 10, Jl. Meruya Ilir Raya No. 88, Kode Pos 11620

Registration Date

Mar 28, 2024

Expiry Date

Oct 19, 2025

Product Type

Surgical Equipment

Ultraviolet lamp for dermatologic disorders.

Non Radiation Electromedics

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