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PROLINE Immunoglobulin E FS - Indonesia BPOM Medical Device Registration

PROLINE Immunoglobulin E FS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305320833. The device is manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRODIA MEDICAL DISTRIBUTION.

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BPOM Registered
Risk Class Kelas Resiko : B
PROLINE Immunoglobulin E FS
Analysis ID: AKL 20305320833

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PRODIA MEDICAL DISTRIBUTION

AR Address

Kawasan Industri Jababeka III, Jalan Tekno 1 Blok C 2 D Lantai 1 Lot 1

Registration Date

May 05, 2023

Expiry Date

May 05, 2026

Product Type

Immunological Test System

Immunoglobulins A, G, M, D, and E immunological test system.

Invitro Diagnostics

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