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VLEDX Double Light - Indonesia BPOM Medical Device Registration

VLEDX Double Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520041. The device is manufactured by KENSWICK GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ASANUS MEDIKA 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
VLEDX Double Light
Analysis ID: AKL 21603520041

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KENSWICK GMBH

Country of Origin

Germany

Authorized Representative

PT. ASANUS MEDIKA INDONESIA

AR Address

CBD Gading Serpong, Ruko Paramount Dotcom Orange No.17

Registration Date

Jan 04, 2025

Expiry Date

Aug 15, 2029

Product Type

Surgical Equipment

Surgical lamp.

Non Radiation Electromedics

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