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XPRESFIX Non-Woven Plaster + Pad - Indonesia BPOM Medical Device Registration

XPRESFIX Non-Woven Plaster + Pad is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902220155. The device is manufactured by ZHEJIANG AOKI MEDICAL DRESSING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GIDION JAYA.

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BPOM Registered
Risk Class Kelas Resiko : A
XPRESFIX Non-Woven Plaster + Pad

XPRESFIX Plester Non-Woven + Pad

Analysis ID: AKL 10902220155

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. GIDION JAYA

AR Address

JL SULTAN HASANUDIN RT 005 / RW 05, AMBON 97128, MALUKU

Registration Date

Jan 15, 2025

Expiry Date

Jan 13, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Medical adhesive tape and adhesive bandage, sterile

Non Electromedic Sterile

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