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COBAS b 101 and Accessories - Indonesia BPOM Medical Device Registration

COBAS b 101 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207312584. The device is manufactured by PANASONIC HEALTHCARE CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
COBAS b 101 and Accessories
Analysis ID: AKL 20207312584

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. ROCHE INDONESIA

AR Address

Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi

Registration Date

May 25, 2022

Expiry Date

Mar 15, 2027

Product Type

Haematology Package and Kit

Glycosylated hemoglobin assay.

Invitro Diagnostics

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