STERILE CARDIOVASCULAR GUIDEWIRE ALAMBRE DE GUÍA CARDIOVASCULAR
- Risk class / Clase de Riesgo
- III
- Product type (Spanish)
- MEDICO QUIRURGICOS
- Product type (English)
- SURGICAL DOCTOR
- Analysis ID
- 81f3d8394abb43befa65c1cc78ec9938
- Expire date
- November 17, 2033
- Name (Spanish)
- NIPRO MEDICAL CORPORATION
- Name (English)
- NIPRO MEDICAL CORPORATION
ALAMBRE DE GUÍA CARDIOVASCULAR DESECHABLE UTILIZADO EN ANGIOPLASTIA CORONARIA TRANSLUMINAL PERCUTÁNEA (PTCA) Y ANGIOPLASTIA TRANSLUMINAL PERCUTÁNEA (PTA) PARA GUIAR CATÉTERES CON BALÓN O SISTEMAS DE STENT AL SITIO DE LA LESIÓN.
DISPOSABLE CARDIOVASCULAR GUIDE WIRE USED IN PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) AND PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) TO GUIDE BALLOON CATHETERS OR STENT SYSTEMS TO THE SITE OF INJURY.
Access comprehensive regulatory information for STERILE CARDIOVASCULAR GUIDEWIRE ALAMBRE DE GUÍA CARDIOVASCULAR (STERILE CARDIOVASCULAR GUIDEWIRE CARDIOVASCULAR GUIDE WIRE ) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 81f3d8394abb43befa65c1cc78ec9938 and manufactured by NIPRO MEDICAL CORPORATION. The device was registered on November 17, 2033.
This page provides complete registration details including product type (SURGICAL DOCTOR), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.