TERUMO Imugard III-RC - Indonesia BPOM Medical Device Registration
TERUMO Imugard III-RC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902211476. The device is manufactured by FUJINOMIYA FACTORY OF TERUMO CORPORATION. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJINOMIYA FACTORY OF TERUMO CORPORATION.Country of Origin
Japan
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Apr 19, 2021
Expiry Date
Mar 02, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
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RADIFOCUS Glidewire Advantage
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SURSHIELD SURFLO II
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CHEMOSAFE LOCK™ Vented Vial Spike, 20mm
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TERUFUSION™ SS 10
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CHEMOSAFE LOCK™ Bag Spike
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Trima Accel® LRS® Platelet, Plasma Set
TFB MANUFACTURING SRL