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EURO-All Silicon Latex Foley Catheter - Indonesia BPOM Medical Device Registration

EURO-All Silicon Latex Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805810415. The device is manufactured by EUROMED FOR MEDICAL INDUSTRIES S.A.E from Egypt, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIPATRIA MAINSTAY MEDIKA.

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 : C
EURO-All Silicon Latex Foley Catheter
Analysis ID: AKL 10805810415

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Egypt

Authorized Representative

PT. TRIPATRIA MAINSTAY MEDIKA

AR Address

Jl Musi No. 37 Jakarta 10150

Registration Date

Dec 17, 2020

Expiry Date

Oct 04, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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