GANSHORN Spirometri & DLCO - Indonesia BPOM Medical Device Registration
GANSHORN Spirometri & DLCO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401220023. 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. MEGA GLOBAL PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GANSHORN MEDIZIN ELECTRONIC GMBHCountry of Origin
Germany
Authorized Representative
PT. MEGA GLOBAL PRATAMAAR Address
JL. Cengkeh Blok 16 No. 11 Kel. Pinangsia Kec. Tamansari Jakarta Barat 11110
Registration Date
Oct 14, 2022
Expiry Date
Sep 13, 2025
Product Type
Diagnostic Anesthesia Equipment
Diagnostic spirometer.
Non Radiation Electromedics
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