Pure Global

RUTILIGHT - Lighting device for surgical instruments - Indonesia BPOM Medical Device Registration

RUTILIGHT - Lighting device for surgical instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325015. The device is manufactured by SWAN MEDICAL S.L from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AMPM HEALTHCARE 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
RUTILIGHT - Lighting device for surgical instruments
Analysis ID: AKL 21603325015

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SWAN MEDICAL S.L

Country of Origin

Spain

Authorized Representative

AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Sep 15, 2023

Expiry Date

Feb 01, 2028

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