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ANSCARE ENT Surgical Sponge - Indonesia BPOM Medical Device Registration

ANSCARE ENT Surgical Sponge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702612802. The device is manufactured by CENEFOM CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : C
ANSCARE ENT Surgical Sponge
Analysis ID: AKL 20702612802

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. PRO-HEALTH INTERNATIONAL

AR Address

Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5

Registration Date

Nov 19, 2020

Expiry Date

Jun 29, 2025

Product Type

Prosthetic Ear, Nose and Throat Equipment

Ear, nose, and throat synthetic polymer material.

Non Electromedic Sterile

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