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EUDAMED last updated this device on May 22, 2026
B-69509960AHPV1801-BSKY7AHPV1801-BOG48E，AHPV1801-BOG96E is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Zhejiang Orient Gene Biotech Co., Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-69509960AHPV1801-BSKY7AHPV1801-BOG48E，AHPV1801-BOG96ED-69509960AHPV1801-BSKY7
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0105041004FULL GENOTYPING HIGH-RISK + LOW-RISK HPV - NA REAGENTSPrimary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
CN-MF-000017965Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →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.
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 →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.
V10 092305 0004SupplementedNotified 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.
CR-04-1249-874-25SupplementedNotified 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.
CR-04-1249-875-25IssuedNotified 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.
No certificate specifically references this device's Basic UDI-DI.
B-69509960SNCE01X59WOn the marketMNAP01-AOGEB-69509960MNAP01VYBBOn the marketSDVS01-AOG50E; SDVS01-BOG50E; SDVS01-COG50E; SDVS01-DOG50EB-69509960SDVS0125DNOn the marketAHSV101-AOG48E; AHSV101-AOG96E; AHSV101D-AOG48E; AHSV101D-AOG96EB-69509960AHSV101W7HFOn the marketSMTB01-AHG5E,SMTB01-AHG25E, SMTB01-BHG5E, SMTB01-BHG25EB-69509960SMTB0125BSOn the marketABPTS02-AOG48E/ ABPTS02-AOG96EB-69509960ABPTS02XHQ3On the market