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GERATHERM Spirometry System Spirostik - Indonesia BPOM Medical Device Registration

GERATHERM Spirometry System Spirostik is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401220007. 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. GLOBAL MEDICAL PRESS.

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BPOM Registered
Risk Class Kelas Resiko : B
GERATHERM Spirometry System Spirostik
Analysis ID: AKL 20401220007

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. 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, 2029

Product Type

Diagnostic Anesthesia Equipment

Monitoring spirometer.

Non Radiation Electromedics

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