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CHRONACARE Latex Foley Catheter - Indonesia BPOM Medical Device Registration

CHRONACARE Latex Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805321001. The device is manufactured by WELL LEAD MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BUANA INTIPRIMA USAHA.

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
CHRONACARE Latex Foley Catheter
Analysis ID: AKL 20805321001

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BUANA INTIPRIMA USAHA

AR Address

Pergudangan Green Lake City, Gudang RCTS Nomor 050, RT/RW: 006/008

Registration Date

Aug 13, 2024

Expiry Date

Aug 12, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Suprapubic urological catheter and accessories.

Non Electromedic Sterile

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