AFENTTA Aspiration Catheter - Indonesia BPOM Medical Device Registration

AFENTTA Aspiration Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505420004. The device is manufactured by WEIHAI HEMO JIRUI BIO-TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : C

AFENTTA Aspiration Catheter

Analysis ID: AKL 20505420004

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

WEIHAI HEMO JIRUI BIO-TECHNOLOGY CO., LTD.

Country of Origin

China

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Jan 11, 2024

Expiry Date

Oct 10, 2026

Product Type

Therapeutic Cardiology Equipment

Embolectomy catheter.

Non Electromedic Sterile

DJ Fang

MedTech Regulatory Expert

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