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BAXTER TruLight 1000 Examination Light - Indonesia BPOM Medical Device Registration

BAXTER TruLight 1000 Examination Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603318058. The device is manufactured by BAXTER MEDICAL SYSTEMS GMBH + CO., KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is IDS MEDICAL SYSTEMS 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
BAXTER TruLight 1000 Examination Light
Analysis ID: AKL 21603318058

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Jun 13, 2024

Expiry Date

Dec 31, 2026

Product Type

Surgical Equipment

Surgical lamp.

Non Radiation Electromedics

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