- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Sep 14, 2026
59079968M04010202H4elastoDERM Foil dressing, self-adhesive, sterile is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by ZARYS International Spółka z ograniczoną odpowiedzialnością . Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
PL-MF-000000410(01)05907996808908
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
3 warnings recorded — scroll inside the panel to see all entries.
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 Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary 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.
05907996808908Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
59079968M04010202H4811210UDI 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.
2 packaging levels registered — each level carries its own UDI-DI.
05907996808908× 1 unitBase unit05907996808915× 100 units05907996808922× 30 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
M04010202POLYURETHANE FIXING DRESSINGSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
HZ 2739190-1RestrictedNotified 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 →59079968M04010202H4On the marketelastoDERM F-IV IV cannula dressing, foil, with frame, with U-incision, self-adhesive, sterile59079968M04010202H4On the marketelastoDERM F-IV IV cannula dressing, foil, with frame, with U-incision, self-adhesive, sterile59079968M04010202H4On the marketelastoDERM Foil dressing, self-adhesive, sterile59079968M04010202H4On the marketelastoDERM Foil dressing, self-adhesive, sterile59079968M04010202H4On the marketelastoDERM Foil dressing, self-adhesive, sterile59079968M04010202H4On the marketNo certificate specifically references this device's Basic UDI-DI.