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TECHNOMED Balloon Dilatation Catheter - Indonesia BPOM Medical Device Registration

TECHNOMED Balloon Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505124846. The device is manufactured by BROSMED MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIPUTRA TECHNO MED.

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BPOM Registered
Risk Class Kelas Resiko : C
TECHNOMED Balloon Dilatation Catheter
Analysis ID: AKL 20505124846

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRIPUTRA TECHNO MED

AR Address

Jl. Metro Tanjung Bunga Ruko Sumba Opu Blok A/17

Registration Date

Aug 05, 2021

Expiry Date

Aug 05, 2024

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

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