ID-DiaCell I-II-III Asia - Indonesia BPOM Medical Device Registration
ID-DiaCell I-II-III Asia is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220301. The device is manufactured by DIAMED GMBH from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAMED GMBHCountry of Origin
Switzerland
Authorized Representative
ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Dec 20, 2022
Expiry Date
Sep 01, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
Invitro Diagnostics
BIO-RAD ID-DiaPanel-P
BIO-RAD ID-DiaCell ABO A1, B
BIO-RAD DiaClon RhD + Phenotype
BIO-RAD ID-Dia (Diego) Positive
DIAMED IH-QC7 Modular System
DIAMED IH-QC3 Modular System
DIAMED IH-QC4 Modular System
DIAMED IH-QC8 Modular System
DIAMED IH-QC6 Modular System
DIAMED IH-QC2 Modular System
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