Pure Global

KLS Martin Operation Light - Indonesia BPOM Medical Device Registration

KLS Martin Operation Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603126213. The device is manufactured by KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. KG, from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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
KLS Martin Operation Light
Analysis ID: AKL 21603126213

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Oct 21, 2022

Expiry Date

Dec 31, 2025

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