Pure Global

LUXAMED Aneroid Sphygmomanometer - Indonesia BPOM Medical Device Registration

LUXAMED Aneroid Sphygmomanometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501124082. The device is manufactured by LUXAMED GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.

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
LUXAMED Aneroid Sphygmomanometer
Analysis ID: AKL 20501124082

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96

Registration Date

Jul 10, 2021

Expiry Date

May 11, 2026

Product Type

Diagnostic Cardiology Equipment

Noninvasive blood pressure measurement system.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing