Pure Global

FemoStop ™ II Plus System Set - Indonesia BPOM Medical Device Registration

FemoStop ™ II Plus System Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504027588. The device is manufactured by ST JUDE MEDICAL PUERTO RICO., LLC from Puerto Rico USA, and is classified as Risk Class Kelas Resiko : B. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
FemoStop ™ II Plus System Set
Analysis ID: AKL 20504027588

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Puerto Rico USA

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5

Registration Date

Dec 07, 2020

Expiry Date

Aug 01, 2024

Product Type

Surgical Cardiology Equipment

Vascular clamp.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from ST JUDE MEDICAL PUERTO RICO., LLC
Products from the same manufacturer (1 products)