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U-Cath Silicon Foley Ballon Catheter - Indonesia BPOM Medical Device Registration

U-Cath Silicon Foley Ballon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420146. The device is manufactured by LA-MED HEALTHCARE PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SINAR PANCA MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
U-Cath Silicon Foley Ballon Catheter
Analysis ID: AKL 20805420146

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

SINAR PANCA MEDIKA

AR Address

Ruko Sedayu Square Blok G-01/G-02, Jl. Lingkar Luar Barat, Kel. Cengkareng Barat, Kec. Cengkareng, Kota Adm. Jakarta Barat, Provinsi DKI Jakarta, Kode Pos 11730

Registration Date

Mar 15, 2024

Expiry Date

Aug 01, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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