SIGVARIS Dynaven Classic AD - Indonesia BPOM Medical Device Registration
SIGVARIS Dynaven Classic AD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902021304. The device is manufactured by SIGVARIS AG. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EURAMED MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SIGVARIS AG.Country of Origin
Switzerland
Authorized Representative
PT. EURAMED MEDICAL INDONESIAAR Address
Komp. Ruko Green Garden Blok Z4 No. 24
Registration Date
Mar 20, 2020
Expiry Date
Nov 06, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
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