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BARD CHIBA Fine Needle Aspiration - Indonesia BPOM Medical Device Registration

BARD CHIBA Fine Needle Aspiration is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801126025. The device is manufactured by CAREFUSION D.R. 203 LTD. from Dominican, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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
BARD CHIBA Fine Needle Aspiration
Analysis ID: AKL 20801126025

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Dominican

Authorized Representative

PT. PRO-HEALTH INTERNATIONAL

AR Address

Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5

Registration Date

May 28, 2022

Expiry Date

Feb 08, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Electromedic Sterile

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