Albania AKBPM registration 14007.0

HemoPill Acute 500.01

Name: HemoPill Acute 500.01 — Albania device registration 14007.0
Creator: Ovesco Endoscopy AG;Friedrich-Miescher-Str.9,D-72076 Tubingen, Germany
Keywords: HemoPill Acute 500.01, HemoPill Acute 500.01, Ovesco Endoscopy AG;Friedrich-Miescher-Str.9,D-72076 Tubingen, Germany, KIasaIIa, Albania medical device

AlbaniaOvesco Endoscopy AG;Friedrich-Miescher-Str.9,D-72076 Tubingen, GermanyKIasaIIaModel HemoPill Acute 500.01

VerifiedAKBPM · official registry

Device classification

Risk Class: KIasaIIa
Product Model: HemoPill Acute 500.01
Product Name: HemoPill Acute 500.01

Registration information

Analysis ID: 14007.0

Manufacturer

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

Product information

Kapsule per detektimin e gjakderdhjeve ne sitemin gastrointestinal

About this record

Access comprehensive regulatory information for HemoPill Acute 500.01 in the Albania medical device market through Pure Global AI's free database. This KIasaIIa 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 (HemoPill Acute 500.01), 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.