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RADISTOP ™ Compression Assist Device - Indonesia BPOM Medical Device Registration

RADISTOP ™ Compression Assist Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11604916986. The device is manufactured by ST. JUDE MEDICAL PUERTO RICO, LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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 : A
RADISTOP ™ Compression Assist Device
Analysis ID: AKL 11604916986

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

RUKAN PERMATA SENAYAN BLOK A18-19 JL. TENTARA PELAJAR NO. 5

Registration Date

Oct 28, 2019

Expiry Date

Aug 01, 2024

Product Type

Therapeutic Surgical Equipment

Nonpneumatic tourniquet.

Non Electromedic Sterile

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