- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jul 22, 2026
42519946GLEITHILFENZTGleitbettlaken ca. 90 x 200 x 12 cm - Mittelteil 100 % Nylon, silikonbeschichtet is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Centre Barbara Schardt e.K.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
DE-MF-000021441(01)04251994650122
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 Germany; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Mar 1, 2011 | Still on market |
| Austria | Mar 1, 2011 | Still on market |
| Luxembourg | Jan 1, 2015 | Still on market |
| Netherlands | Jan 1, 2015 | 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.
04251994650122Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
42519946GLEITHILFENZT51176UDI 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.
Z12019010PATIENT TRANSFER SYSTEMSPrimary 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.
No 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.42519946GLEITHILFENZTOn the marketCentre Gleittuch mit Griffen, ca. 45 × 140 cm, 100 % Nylon, silikonbeschichtet42519946GLEITHILFENZTOn the marketCentre Tunnelgleithilfe, ca. 90 × 70 cm, offen auf 70 cm, 100 % Nylon, silikonbeschichtet42519946GLEITHILFENZTOn the marketGleittuch Softline ca. 90 x 140 cm mit Griffen, 100 % PES, silikonbeschichtet beidseitig42519946GLEITHILFENZTOn the marketMini Tunnelgleithilfe Softline 2er Set ca 30 cm x 35 cm, 100 % PES, silikonbeschichtet beidseitig42519946GLEITHILFENZTOn the marketMini-Tunnelgleithilfe, 2er Set ca. 30 x 35 cm- offen auf 35 cm, 100 % Nylon, silikonbeschichtet42519946GLEITHILFENZTOn the market