651-128Percutaneous Endoscopic Gastrostomy Kit
Argentina Medical Device Registration · EndoVive · BOSTON SCIENTIFIC ARGENTINA S.A. · Registered June 23, 2024
Registration modification (non-agile) Class III-IV- Registration Type
- Registration modification (non-agile) Class III-IV
- Modificación de Registro (no ágil) Clase III-IV
- Product Code
- 651-128
- Brand Name
- EndoVive
- Product Name
- Percutaneous Endoscopic Gastrostomy Kit
- Kit para gastrostomía endoscópica percutánea
- Registration Date
- June 23, 2024
- Database ID
- cmhaytq4e07lqekuzuucjjrom
M00568401 20 Fr Percutaneous Endoscopic Gastrostomy Kit, Push M00568411 24 Fr Percutaneous Endoscopic Gastrostomy Kit, Push M00568381 20 Fr Percutaneous Endoscopic Gastrostomy Kit, Pull M00568391 24 Fr Percutaneous Endoscopic Gastrostomy Kit, Pull
M00568401 20 Fr Kit para gastrostomía endoscópica percutánea, Push M00568411 24 Fr Kit para gastrostomía endoscópica percutánea, Push M00568381 20 Fr Kit para gastrostomía endoscópica percutánea, Pull M00568391 24 Fr Kit para gastrostomía endoscópica percutánea, Pull
Access comprehensive regulatory information for Percutaneous Endoscopic Gastrostomy Kit in the Argentina medical device market through Pure Global AI's free database. This Registration modification (non-agile) Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 23, 2024.
This page provides complete registration details including product code (651-128), brand name (EndoVive), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.