Speedpass ™ Aspiration Catheter - Indonesia BPOM Medical Device Registration
Speedpass ™ Aspiration Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505420041. 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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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
Therapeutic Cardiology Equipment
Embolectomy catheter.
Non Electromedic Sterile
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