TERUMO PENPOL Blood Collection Monitor D 601 - Indonesia BPOM Medical Device Registration
TERUMO PENPOL Blood Collection Monitor D 601 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209029581. The device is manufactured by TERUMO PENPOL PRIVATE LIMITED. from India, 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
TERUMO PENPOL PRIVATE LIMITED.Country of Origin
India
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Dec 26, 2020
Expiry Date
Aug 14, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood mixing devices and blood weighing devices.
Invitro Diagnostics
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