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PUHUI Micro Guidewire - Indonesia BPOM Medical Device Registration

PUHUI Micro Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501520004. The device is manufactured by SHANGHAI PUHUI MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REKAMILENIUMINDO SELARAS.

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
PUHUI Micro Guidewire
Analysis ID: AKL 20501520004

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. REKAMILENIUMINDO SELARAS

AR Address

Jl.Tomang Raya No 51B

Registration Date

Jan 03, 2025

Expiry Date

Mar 05, 2029

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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