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FESCO All Silicone Foley Catheter (2 ways) - Indonesia BPOM Medical Device Registration

FESCO All Silicone Foley Catheter (2 ways) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805321072. The device is manufactured by WELL LEAD MEDICAL CO., LTD., CHINA from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FESCO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
FESCO All Silicone Foley Catheter (2 ways)
Analysis ID: AKL 20805321072

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FESCO INDONESIA

AR Address

RUKO MEGA GROSIR CEMPAKA MAS BLOK E 1/17 Jalan Letjend Suprapto Rt 07 Rw 08, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Kemayoran, Kel. Sumur Batu

Registration Date

Dec 17, 2023

Expiry Date

Dec 14, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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