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SURGIKAR Disposable Silicone Foley Catheter - Indonesia BPOM Medical Device Registration

SURGIKAR Disposable Silicone Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220221. The device is manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.

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Risk Class Kelas Resiko : C
SURGIKAR Disposable Silicone Foley Catheter
Analysis ID: AKL 20805220221

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Nov 03, 2023

Expiry Date

Nov 02, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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