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MERIT Manifold - Indonesia BPOM Medical Device Registration

MERIT Manifold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504320165. The device is manufactured by MERIT MEDICAL SYSTEMS, INC, from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REKAMILENIUMINDO IN ACCORDANCE.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
MERIT Manifold
Analysis ID: AKL 20504320165

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

REKAMILENIUMINDO IN ACCORDANCE

AR Address

Jl. Tomang Raya No. 51B RT 01 RW 05, Kelurahan Tomang

Registration Date

Jun 26, 2023

Expiry Date

Dec 31, 2025

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.

Non Electromedic Sterile

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