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PLASTI-MED Ureteral Catheter - Indonesia BPOM Medical Device Registration

PLASTI-MED Ureteral Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805125180. The device is manufactured by PLASTI-MED PLASTIC MEDICAL URUNLER SAN. TIC. LTD. ST. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EDISON AMBASSADOR MEANS.

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
PLASTI-MED Ureteral Catheter
Analysis ID: AKL 20805125180

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. EDISON AMBASSADOR MEANS

AR Address

Jl. Oasis Sememi Raya No. 1 RT 05 RW 04, Kel. Sememi, Kec. Benowo, Surabaya, Jawa Timur

Registration Date

Feb 22, 2024

Expiry Date

Dec 08, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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