SEWOON All Silicone Penrose Drainage Tube - Indonesia BPOM Medical Device Registration

SEWOON All Silicone Penrose Drainage Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805904100. The device is manufactured by SEWOON MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PRIMA ALKESINDO NUSANTARA.

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BPOM Registered

Risk Class Kelas Resiko : C

SEWOON All Silicone Penrose Drainage Tube

Analysis ID: AKL 20805904100

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SEWOON MEDICAL CO., LTD.

Country of Origin

Korea

Authorized Representative

PRIMA ALKESINDO NUSANTARA

AR Address

Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

Oct 21, 2022

Expiry Date

Jul 28, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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