HANSAPLAST Transparent - Indonesia BPOM Medical Device Registration
HANSAPLAST Transparent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902412540. 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 PT. BEIERSDORF INDONESIA.
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HANSAPLAST Transparan
Risk Classification
Product Class
Kelas : 1
Manufacturer
BEIERSDORF MANUFACTURING ARGENTONA, S.LCountry of Origin
Spain
Authorized Representative
PT. BEIERSDORF INDONESIAAR Address
South Quarter Tower C lantai 6 Jl. R.A. Kartini kav.8, Cilandak Barat, Cilandak, Jakarta selatan, DKI Jakarta, 12430
Registration Date
Jul 29, 2024
Expiry Date
Jan 25, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Elastic bandage.
Non Electromedic Non Sterile
HANSAPLAST Second Skin Protection
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HANSAPLAST Soft Compress Steril
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HANSAPLAST Kasa Sterile
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HANSAPLAST Marvel
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HANSAPLAST Wound Ointment
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HANSAPLAST Gauze Elastic Roller
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HANSAPLAST Aqua Protect Sterile
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HANSAPLAST Sensitive Sterile
BEIERSDORF MANUFACTURING ARGENTONA S.L.

