RESECT+ AQANIFE,AqaNife 200.53.01/200.53.02/200.53.03/200.53.04

Albania medical device registration · Ovesco Endoscopy AG;Friedrich-Miescher-Str.9,D-72076 Tubingen, Germany · KIasaIIb · Model RESECT+ AQANIFE,AqaNife 200.53.01/200.53.02/200.53.03/200.53.04

Device classification

Risk Class: KIasaIIb
Product Model: RESECT+ AQANIFE,AqaNife 200.53.01/200.53.02/200.53.03/200.53.04
Product Name: RESECT+ AQANIFE,AqaNife 200.53.01/200.53.02/200.53.03/200.53.04

Registration information

Analysis ID: 14012.0

Manufacturer

Name: Ovesco Endoscopy AG;Friedrich-Miescher-Str.9,D-72076 Tubingen, Germany

Product information

Elektrode monopolare per prerjen e shtreses submukozale

About this record

Access comprehensive regulatory information for RESECT+ AQANIFE,AqaNife 200.53.01/200.53.02/200.53.03/200.53.04 in the Albania medical device market through Pure Global AI's free database. This KIasaIIb medical device is manufactured by Ovesco Endoscopy AG;Friedrich-Miescher-Str.9,D-72076 Tubingen, Germany.

This page provides complete registration details including product model (RESECT+ AQANIFE,AqaNife 200.53.01/200.53.02/200.53.03/200.53.04), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.