Pure Global

ASETRONICS ASELight 120 - Indonesia BPOM Medical Device Registration

ASETRONICS ASELight 120 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603715908. The device is manufactured by ASETRONICS AT from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DEMKA SAKTI.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
ASETRONICS ASELight 120
Analysis ID: AKL 21603715908

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ASETRONICS AT

Country of Origin

Switzerland

Authorized Representative

DEMKA SAKTI

AR Address

JLN. TANAH ABANG III/19 A-B, RT.002/RW.003

Registration Date

Jan 08, 2025

Expiry Date

Dec 31, 2029

Product Type

Surgical Equipment

Surgical lamp.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing