HANSAPLAST Plastic - Indonesia BPOM Medical Device Registration
HANSAPLAST Plastic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902412539. The device is manufactured by BEIERSDORF MANUFACTURING ARGENTONA S.L from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BEIERSDORF INDONESIA.
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HANSAPLAST Plastik
Risk Classification
Product Class
Kelas : 1
Manufacturer
BEIERSDORF MANUFACTURING ARGENTONA S.LCountry of Origin
Spain
Authorized Representative
BEIERSDORF INDONESIAAR Address
Jl. Raya Randuagung KM. 75. Singosari
Registration Date
Mar 03, 2021
Expiry Date
Dec 13, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Elastic bandage.
Non Electromedic Non Sterile
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