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EUDAMED last updated this device on Jun 4, 2026
7330530DW001KJPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →A2M STAF 100X30 OA M BROMS is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Haco Tellus AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →07330530006757Basic 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 →7330530DW001KJM3000006UDI 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 →(01)07330530006757
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Y122499WHEELCHAIRS ACCESSORIES - OTHERSterile
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 →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Sweden; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Jan 1, 2024 | Still on market |
SE-MF-000053610No 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.7330530CW001K7On the marketA2M STAF 150X30 OA M BROMS7330530DW001KJOn the marketA2M-NEK 100X32 OA 10 MM BÄRF 80 KG7330530MF001JWOn the marketA2M-NEK 125X32 OA 10 MM BÄRF 100 KG7330530MF001JWOn the marketA2M-NEK 125X32 OA 10 MM BÄRF 100 KG7330530MF001JWOn the market