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BARDIA Foley Catheter - Indonesia BPOM Medical Device Registration

BARDIA Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805502873. The device is manufactured by BARD SDN BHD from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SCINTILLATING ASIAN CENTER.

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BPOM Registered
Risk Class Kelas Resiko : C
BARDIA Foley Catheter
Analysis ID: AKL 20805502873

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

BARD SDN BHD

Country of Origin

Malaysia

Authorized Representative

PT. SCINTILLATING ASIAN CENTER

AR Address

JL. Pantai Indah Barat, Komplek TOHO Pantai Indah Kapuk Blok H 25 & 27, Kamal Muara - Penjaringan Jakarta Utara

Registration Date

Jul 06, 2021

Expiry Date

Sep 30, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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