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SERENITY Urethral Catheter - Indonesia BPOM Medical Device Registration

SERENITY Urethral Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805111160. The device is manufactured by ZHANJIANG STAR ENTERPRISE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SERENITY INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
SERENITY Urethral Catheter
Analysis ID: AKL 20805111160

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SERENITY INDONESIA

AR Address

Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01

Registration Date

Jul 26, 2023

Expiry Date

Feb 07, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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