- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Mar 30, 2026
B-G451CSS22073NMV1500AB is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Arctic Solutions Inc., dba Custom Biogenic Systems. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
US-MF-000034307CE 725606G451CSS22073NM
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Austria; available across 13 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Sep 23, 2005 | Still on market |
| Belgium | Sep 23, 2005 | Still on market |
| Denmark | Sep 23, 2005 | Still on market |
| EL | Sep 23, 2005 | Still on market |
| Spain | Sep 23, 2005 | Still on market |
| France | Sep 23, 2005 | Still on market |
| Ireland | Sep 23, 2005 | Still on market |
| Italy | Sep 23, 2005 | Still on market |
| Luxembourg | Sep 23, 2005 | Still on market |
| Netherlands | Sep 23, 2005 | Still on market |
| Portugal | Sep 23, 2005 | Still on market |
| Sweden | Sep 23, 2005 | Still on market |
| XI | Sep 23, 2005 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
G451CSS22073NMBasic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-G451CSS22073NMV1500ABUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHERPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
This device is not currently linked to any other device.
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.