- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 15, 2026
8806712BGMS006T5mylife Aveo Blood Glucose Monitoring System is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class C. Manufactured by i-SENS, Inc.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08806712005607700026281KR-MF-000009173V76 090700 0062(01)08806712005607
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Primary placement in Germany; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
| Denmark | — | Still on market |
| Finland | — | Still on market |
| Norway | — | Still on market |
| Sweden | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0201060102BLOOD GLUCOSE METERSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
V76 090700 0062SupplementedV13 090700 0058SupplementedG10 090700 0039SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →8806712BGMME006VXOn the marketmylife Aveo Blood Glucose Meter8806712BGMME006VXOn the marketmylife Aveo Blood Glucose Monitoring System8806712BGMS006T5On the marketmylife Aveo Blood Glucose Monitoring System8806712BGMS006T5On the marketmylife Aveo Blood Glucose Monitoring System8806712BGMS006T5On the marketmylife Aveo Blood Glucose Test Strips8806712BGMTS0083MOn the market