- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 28, 2026
59020960SW-PRNRPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →160/240 - SW-PR-160/240 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Zakład Produkcji Pościeli "ŚWIT" Izabela Wintoniak. Placed on the EU market in Poland. 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 →5902096001266Basic 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 →59020960SW-PRNR160/240 - SW-PR-160/240UDI 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 →5902096001266
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
T020199SURGICAL DRAPES - 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 Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Apr 28, 2026 | Dec 31, 2029 |
PL-MF-000043811No 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.59020960SW-POSZTROn the market100/160 - SW-PR-100/16059020960SW-PRNROn the market100/200 – SW-PR-100/200 + gumka59020960SW-PRNROn the market140/200 - SW-POSZ-140/200 + zakładka 30 cm59020960SW-POSZTROn the market150/210- SW-PR-150/21059020960SW-PRNROn the market