TYSHAK II Percutaneous Valvuloplasty Catheter - Indonesia BPOM Medical Device Registration
TYSHAK II Percutaneous Valvuloplasty Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320640. The device is manufactured by NUMED, INC. from United States, and is classified as Risk Class Kelas Resiko : C. 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
NUMED, INC.Country of Origin
United States
Authorized Representative
NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Oct 10, 2024
Expiry Date
Dec 31, 2028
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
TACTICATHโข Contact Force Ablation Catheter, Sensor Enabledโข
ABBOTT MEDICAL
Z-MED II โข Percutaneous Transluminal Valvulopasty Catheter
NUMED INC.
NUCLEUS Percutaneous Transluminal Valvuloplasty Catheter
NUMED, INC.
TYSHAK Mini Pediatric Valvuloplasty Catheter
NUMED, INC.
Z-5 โข Atrioseptostomy Catheter
NUMED INC.
TYSHAK Percutaneous Transluminal Valvuloplasty Catheter
NUMED, INC.
Fast Cath โข Hemostasis Introducer
ABBOTT MEDICAL
SWARTZ โข Braided Transseptal Guiding Introducer
ABBOTT MEDICAL
Ensite Precision โข Surface Electrode Kit
ABBOTT MEDICAL COSTA RICA LTDA.
BEGRAFT Aortic Stent Graft System
BENTLEY INNOMED GMBH

