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DELVI CARE 2 Way Latex Foley Catheter - Indonesia BPOM Medical Device Registration

DELVI CARE 2 Way Latex Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805520051. The device is manufactured by JIANGXI YIKANG MEDICAL INSTRUMENT GROUP CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DELVI PRIMATAMA.

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BPOM Registered
Risk Class Kelas Resiko : C
DELVI CARE 2 Way Latex Foley Catheter
Analysis ID: AKL 20805520051

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DELVI PRIMATAMA

AR Address

Perum Mutiara Gading Timur Blok A8 No. 7-8 RT 001 RW 031 Kelurahan Mustika Jaya, Kecamatan Mustika Jaya - Kota Bekasi

Registration Date

Feb 10, 2025

Expiry Date

Dec 08, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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