MERIT Manifold 500 PSI - Indonesia BPOM Medical Device Registration
MERIT Manifold 500 PSI is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504615464. 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 PT. MURSMEDIC.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
MERIT MEDICAL SYSTEMS INC.Country of Origin
United States
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Nov 17, 2021
Expiry Date
Dec 31, 2024
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Non Electromedic Sterile
INTUITIVE SURGICAL DA VINCI XI ENDOSCOPIC INSTRUMENT CONTROL SYSTEM AND ACCESSORIES
INTUITIVE SURGICAL INC.
FISHER & PAYKEL Optiflow Tracheostomy Direct Connection
FISHER & PAYKEL HEALTHCARE LTD.
FISHER & PAYKEL Optiflow + Nasal Cannula
FISHER & PAYKEL HEALTHCARE LTD.
FISHER & PAYKEL AIRVO 2 Heated Breathing Tube and Chamber Kit
FISHER & PAYKEL HEALTHCARE LTD.
FISHER & PAYKEL Heated Respiratory Humidifier
FISHER & PAYKEL HEALTHCARE LTD.
FISHER & PAYKEL Optiflow Junior Tubing Kit
FISHER & PAYKEL HEALTHCARE LTD.
IPS Empress® Direct
IVOCLAR VIVADENT AG.
FISHER & PAYKEL Bubble CPAP System and Accessories
FISHER & PAYKEL HEALTHCARE LTD.
SR Triplex Cold
IVOCLAR VIVADENT AG
IPS E.MAX® Ceram
IVOCLAR VIVADENT AG.