Pure Global

SCHILLER Spirometry - Indonesia BPOM Medical Device Registration

SCHILLER Spirometry is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401320031. The device is manufactured by GANSHORN MEDIZIN ELECTRONIC GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.

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
SCHILLER Spirometry
Analysis ID: AKL 20401320031

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Feb 07, 2023

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name
Other Products from GANSHORN MEDIZIN ELECTRONIC GMBH
Products from the same manufacturer (2 products)