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Easytork ™ Guidewire - Indonesia BPOM Medical Device Registration

Easytork ™ Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420198. The device is manufactured by GUANGZHOU EASYCESS MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AKSATA MARGA MAKMUR.

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BPOM Registered
Risk Class Kelas Resiko : C
Easytork ™ Guidewire
Analysis ID: AKL 20501420198

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. AKSATA MARGA MAKMUR

AR Address

Foresta Business Loft 6 Unit 1, BSD City

Registration Date

Apr 01, 2024

Expiry Date

Feb 13, 2029

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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