Pure Global

SWARTZ ™ Braided Transseptal Guiding Introducer - Indonesia BPOM Medical Device Registration

SWARTZ ™ Braided Transseptal Guiding Introducer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501122450. The device is manufactured by ABBOTT MEDICAL from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is NUGRA KARSERA.

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
SWARTZ ™ Braided Transseptal Guiding Introducer
Analysis ID: AKL 20501122450

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ABBOTT MEDICAL

Country of Origin

United States

Authorized Representative

NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Oct 11, 2024

Expiry Date

Feb 06, 2029

Product Type

Diagnostic Cardiology Equipment

Catheter introducer

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing