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SFRI Diluterge H18 - Indonesia BPOM Medical Device Registration

SFRI Diluterge H18 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10208800476. The device is manufactured by SFRI SARL. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MITRA BAHAGIA CITRA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
SFRI Diluterge H18
Analysis ID: AKL 10208800476

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SFRI SARL.

Country of Origin

France

Authorized Representative

PT. MITRA BAHAGIA CITRA MEDIKA

AR Address

Jl. Raya Kalirungkut 27 Blok C-63

Registration Date

Oct 08, 2023

Expiry Date

Aug 29, 2028

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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