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POLYFLEX IV Cannula with Injection Port - Indonesia BPOM Medical Device Registration

POLYFLEX IV Cannula with Injection Port is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902705390. The device is manufactured by POLY MEDICURE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEGAH MEDIKA PHARMA.

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BPOM Registered
Risk Class Kelas Resiko : C
POLYFLEX IV Cannula with Injection Port
Analysis ID: AKL 20902705390

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. MEGAH MEDIKA PHARMA

AR Address

Jl. Minangkabau Timur Raya No. 07 RT 006 RW 008

Registration Date

Jan 30, 2025

Expiry Date

Mar 31, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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