SENTINEL Lp(a) Ultra - Indonesia BPOM Medical Device Registration

SENTINEL Lp(a) Ultra is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220404. The device is manufactured by SENTINEL CH. SPA from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

SENTINEL Lp(a) Ultra

Analysis ID: AKL 20101220404

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SENTINEL CH. SPA

Country of Origin

Italy

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta

Registration Date

Mar 30, 2022

Expiry Date

Jan 11, 2025

Product Type

Clinical Chemistry Test System

Lipoprotein test system (kit & cair)

Invitro Diagnostics

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Products from the same manufacturer (10 products)

SENTINEL Lp(a) Ultra - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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