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EUDAMED last updated this device on May 26, 2026
84356058UDI-DI-005WDRY SWAB – Polystyrene + viscose is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Deltalab, S.L.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0843526384396570122001101 packaging level registered — each level carries its own UDI-DI.
08435263843965× 4 unitsBase unit08435263843972× 500 units(01)08435263843965
European Medical Device Nomenclature — the EU product classification assigned to this device.
A1101SAMPLE COLLECTION NEUTRAL SWABS1 warning recorded — scroll inside the panel to see all entries.
1. If it appears that the unitary packaging has lost its integrity, do not use the swab as there is no guarantee of its sterility. 2. Do not use in case of missing component or the product information is not displayed correctly. 3. Discard the product if you find any broken, dirt, chipped, loose tips and/or tipless swab. 4. Do not use if expiry date has been overcome. 7. For single use. The reuse of this product may cause infections. 8. Handle carefully. Any strong pressure during use, although unlikely, could break the swab. In case of damage, discard immediately. 10. Not suitable for any other application than its intended use. 11. For pediatric use it is recommended to use swabs with plastic handle. 12. The use of the swab presents no difficulty for the intended end users. 13. After use, the swabs must be decontaminated or treated as contaminated medical waste. It is the responsibility of each laboratory to handle, treat and dispose the waste according to the regulations. Unused swabs can be considered non-hazardous products and can be disposed of accordingly.
ES-MF-000000153The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | — | Still on market |
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.
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 →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 →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.
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 →No certificate specifically references this device's Basic UDI-DI.
84356058UDI-DI-156BOn the marketCYTOLOGY BRUSH84356058UDI-DI-1265On the marketCYTOLOGY BRUSH PEEL PACK84356058UDI-DI-0364On the marketE.S.R.PIPETTE SELF-LEVELLING84356058UDI-DI-166DOn the marketEDTA TUBE DI-K 4ML PP84356058UDI-DI-166DOn the marketEDTA TUBE TRI-K 1ML PP 12X55MM C/PRE-PERF.84356058UDI-DI-166DOn the marketCertificate health across this manufacturer's portfolio.
2024 PR 0038IssuedNotified 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.
View in glossary →