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CANNOFIX- PU, IV Cannula Fixation Polyurethane - Indonesia BPOM Medical Device Registration

CANNOFIX- PU, IV Cannula Fixation Polyurethane is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902212911. The device is manufactured by PHARMAPLAST S.A.E from Egypt, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOBAL DISPOMEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : A
CANNOFIX- PU, IV Cannula Fixation Polyurethane
Analysis ID: AKL 10902212911

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

PHARMAPLAST S.A.E

Country of Origin

Egypt

Authorized Representative

PT. GLOBAL DISPOMEDIKA

AR Address

Jl. Penjernihan 1 No. 38 Lt. 2

Registration Date

Jul 10, 2023

Expiry Date

Jan 06, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter securement device.

Non Electromedic Sterile

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