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GERATHERM Desktop Spirometer - Indonesia BPOM Medical Device Registration

GERATHERM Desktop Spirometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401220002. The device is manufactured by GERATHERM RESPIRATORY GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERSADA MEDIKA SOLUSINDO.

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
GERATHERM Desktop Spirometer
Analysis ID: AKL 20401220002

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PERSADA MEDIKA SOLUSINDO

AR Address

Jl. Raya Cimatis Kav No. 2/80 B (Ruko) RT.002 RW.007 Kelurahan Jatikarya Kec. Jatisampurna Kota Bekasi.

Registration Date

Jan 29, 2022

Expiry Date

Jan 09, 2025

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

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