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REMEL RapID Yeast Plus System - Indonesia BPOM Medical Device Registration

REMEL RapID Yeast Plus System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20302911553. The device is manufactured by REMEL INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.

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BPOM Registered
Risk Class Kelas Resiko : B
REMEL RapID Yeast Plus System
Analysis ID: AKL 20302911553

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REMEL INC.

Country of Origin

United States

Authorized Representative

PT. DIPA PUSPA LABSAINS

AR Address

Dipa Strategic Office, Lantai Lobby, Jl. Raya Kebayoran Lama No.28 RT.009/RW.011, Kel. Grogol Utara, Kec. Kebayoran Lama

Registration Date

Dec 26, 2022

Expiry Date

Oct 05, 2025

Product Type

Microbiology Equipment

Microorganism differentiation and identification device.

Invitro Diagnostics

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