EVE IN - Indonesia BPOM Medical Device Registration
EVE IN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403611105. The device is manufactured by FRITZ STEPHAN GMBH MEDIZINTECHNIK from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HOSPI MEDIK INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FRITZ STEPHAN GMBH MEDIZINTECHNIKCountry of Origin
Germany
Authorized Representative
PT. HOSPI MEDIK INDONESIAAR Address
Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520
Registration Date
Sep 19, 2024
Expiry Date
Aug 01, 2025
Product Type
Therapeutic Anesthesia Equipment
Continuous ventilator.
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