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EUDAMED last updated this device on Jun 13, 2026
40548580151V0101MSPointed Swabs 10 cm, with thread, x-ray, 20 threads, non-sterile is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Fuhrmann GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
DE-MF-000006652(01)04054858345185
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
CW009CW007Sterile
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 Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | 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.
04054858345185Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
40548580151V0101MS50652-HABUDI 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.
M020199COTTON GAUZES - 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.
40548580122V2101M2On the marketPointed swabs 10 cm, 20 threads, à 2 pcs, sterile40548580123V0201M6On the marketPointed Swabs 10 cm, with thread, x-ray, 20 threads, bundle of 10 pcs, non-sterile40548580151V0101MSOn the marketPointed swabs 13 cm, 20 threads, à 5 pcs, sterile40548580123V0201M6On the marketPointed swabs 13 cm, 20 threads, non-sterile40548580111V0201KTOn the marketPointed swabs 13 cm, 20 threads, non-sterile40548580111V0201KTOn the marketNo 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.