ID-Diluent 1 - Indonesia BPOM Medical Device Registration
ID-Diluent 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320429. The device is manufactured by DIAMED GMBH from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAMED GMBHCountry of Origin
Switzerland
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Feb 09, 2023
Expiry Date
Sep 01, 2025
Product Type
Hematological Reagents
Blood cell diluents
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
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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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SONOVA AT
PHONAK TERRA+ BTE-M
SONOVA AT
PHONAK TERRA BTE-M
SONOVA AT
PHONAK TERRA+ BTE-UP
SONOVA AT