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VITRO STD Direct Flow Chip Kit (PCR Reagents) - Indonesia BPOM Medical Device Registration

VITRO STD Direct Flow Chip Kit (PCR Reagents) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027804. The device is manufactured by VITRO S.A. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA MEGATAMA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
VITRO STD Direct Flow Chip Kit (PCR Reagents)
Analysis ID: AKL 20303027804

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

VITRO S.A.

Country of Origin

Spain

Authorized Representative

PT. GRAHA MEGATAMA INDONESIA

AR Address

BIZ PARK 3 COMMERCIAL ESTATE BLOK E NOMOR 9, JALAN SULTAN AGUNG KM 28.5

Registration Date

Feb 01, 2025

Expiry Date

Apr 28, 2027

Product Type

Serological Reagents

Chlamydia serological reagents.

Invitro Diagnostics

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