Mixi Bags 150P - Indonesia BPOM Medical Device Registration
Mixi Bags 150P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902022971. The device is manufactured by HEGEWALD MEDIZINPRODUKTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTI RAY ADAMAR.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HEGEWALD MEDIZINPRODUKTE GMBHCountry of Origin
Germany
Authorized Representative
MULTI RAY ADAMARAR Address
Ruko Gading Bukit Indah Jl. Bukit Gading Raya L-27 Kelapa Gading, Jakarta Utara
Registration Date
Nov 24, 2023
Expiry Date
Dec 31, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
I.V. container.
Non Electromedic Sterile
