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GERATHERM Spirostik Complete - Indonesia BPOM Medical Device Registration

GERATHERM Spirostik Complete is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401220008. 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 GLOBAL MEDICAL PRESS.

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 Spirostik Complete
Analysis ID: AKL 20401220008

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

GLOBAL MEDICAL PRESS

AR Address

Jl. Raya Kebon Jeruk No.26 RT.011 RW.002, Kelurahan Kebon Jeruk, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

Mar 28, 2024

Expiry Date

Feb 20, 2027

Product Type

Diagnostic Anesthesia Equipment

Monitoring spirometer.

Non Radiation Electromedics

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