Tendigo - Indonesia BPOM Medical Device Registration
Tendigo is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302915529. The device is manufactured by FUJIREBIO EUROPE N.V. from Belgium, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FUJIREBIO EUROPE N.V.Country of Origin
Belgium
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Jan 09, 2024
Expiry Date
Mar 21, 2028
Product Type
Microbiology Equipment
Microbiological incubator.
Invitro Diagnostics
INNO-LiPA HPV Genotyping Extra II Amp <20T, CE>
INNO-LiPA HPV Genotyping Extra II <20T,CE>
INNO-LIA HIV I/II Score
INNOTEST ฮฒ-AMYLOID(1-40)
INNOTEST PHOSPHO-TAU (181P)
INNO-LIA HCV Score
INNOTEST ฮฒ-AMYLOID(1-42)
INNOTEST hTau Ag
LiRAS for LiPA HPV v3
ADVIA Centaur Squamous Cell Carcinoma Calibrator (SCC CAL)
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PERMEADERM Biosynthetic Wound Matrix
TRELLEBORG SEALING SOLUTIONS US, INC.
PERMEADERM Biosynthetic Wound Matrix
TRELLEBORG SEALING SOLUTIONS US, INC.
PHONAK TERRA+ RIC-312
SONOVA AT
PHONAK TERRA+ BTE-M
SONOVA AT
PHONAK TERRA BTE-M
SONOVA AT
PHONAK TERRA+ BTE-UP
SONOVA AT