LEON - Indonesia BPOM Medical Device Registration
LEON is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403126621. The device is manufactured by LOWENSTEIN MEDICAL SE & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MITRA MEDITRANS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LOWENSTEIN MEDICAL SE & CO. KG.Country of Origin
Germany
Authorized Representative
PT. MITRA MEDITRANS INDONESIAAR Address
Jl Duri No. 2A jakarta Pusat
Registration Date
Nov 04, 2021
Expiry Date
Jun 18, 2026
Product Type
Therapeutic Anesthesia Equipment
Gas machine for anesthesia or analgesia.
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