- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jan 19, 2026
89080201395835BTrueprep® AUTO Universal Sample Pre-treatment Pack is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Molbio Diagnostics Limited. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0890802013991060205AB05, 60205AB20, 60205AB25, 60205AB503 packaging levels registered — each level carries its own UDI-DI.
08908020139910× 1 unitBase unit08908007989927× 20 units08908020139583× 25 units08908007989934× 50 unitsIN-MF-000028386(01)08908020139910
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
4 warnings recorded — scroll inside the panel to see all entries.
Avoid exposure to sunlight or elevated temperatures (above recommended levels)
OTHER
OTHER
OTHER
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 Belgium; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0105900101REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUSPrimary 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 →890802013959058On the marketTrueprep® AUTO Universal Cartridge Based Sample Prep Kit8908007989880D4On the marketTrueprep® AUTO Universal Sample Pre-treatment Pack89080201395835BOn the marketTrueprep® AUTO v28908007989972DAOn the marketTrueprep® AUTO v2 Universal Cartridge Based Sample Prep Kit8908007989859DDOn the marketNo certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.