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RUSCH - Imex 2 Way Latex Foley Balloon Catheter - Indonesia BPOM Medical Device Registration

RUSCH - Imex 2 Way Latex Foley Balloon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805711210. The device is manufactured by TELEFLEX MEDICAL PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : C
RUSCH - Imex 2 Way Latex Foley Balloon Catheter
Analysis ID: AKL 20805711210

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47, RT.014, RW.003, Desa/Kelurahan Terban, Kecamanan Gondokusuman, Kota Yogyakarta, Provinsi Daerah Istimewa Yogyakarta, Kode Pos : 55223

Registration Date

Nov 13, 2023

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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