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LMB LUXOMATIC V2 Blood Separation Press and accessories - Indonesia BPOM Medical Device Registration

LMB LUXOMATIC V2 Blood Separation Press and accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209712722. The device is manufactured by LMB TECHNOLOGIE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
LMB LUXOMATIC V2 Blood Separation Press and accessories
Analysis ID: AKL 20209712722

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Oct 02, 2024

Expiry Date

Dec 14, 2028

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated blood cell separator

Invitro Diagnostics

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