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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGZHOU EASYCESS MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. AKSATA MARGA MAKMURAR 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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