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TechnoMed Angioflow - Indonesia BPOM Medical Device Registration

TechnoMed Angioflow is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320890. The device is manufactured by SHENZHEN ANTMED CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIPUTRA TECHNO MED.

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.

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BPOM Registered
Risk Class Kelas Resiko : C
TechnoMed Angioflow
Analysis ID: AKL 20501320890

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

Jul 13, 2023

Expiry Date

Jul 13, 2026

Product Type

Diagnostic Cardiology Equipment

Angiographic Injector and Syringe

Non Radiation Electromedics

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