- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Oct 29, 2025
871897113400L5Papillon Twin HR AD matras incl. hoes inco blauw 3zr 90 x 200 x 15 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Deron B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0871897105943013400(01)08718971059430
European Medical Device Nomenclature — the EU product classification assigned to this device.
V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSESNL-MF-000006051The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Netherlands; available across 1 country total.
Placed on the market in Netherlands; per-country availability dates not published.
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 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.871897116300LMOn the marketPapillon Deluxe HR AD matras incl. hoes inco blauw/groen 3zr + opdr. 'This side up' 90 x 200 x 18871897113530LKOn the marketPapillon HR matras incl. hoes inco blauw 3zr 90 x 200 x 15871897110300KBOn the marketPresstige koudschuim matras incl. hoes inco blauw 3zr 90 x 200 x 15871897110500KMOn the marketPresstige traagschuim Deluxe Firm matras incl. hoes inco blauw/groen 3zr + opdr. 'This side up' 90 x 200 x 19871897115430LUOn the marketPresstige traagschuim Deluxe Medium matras incl. hoes inco blauw/groen 3zr + opdr. 'This side up' 90 x 200 x 19871897115330LPOn the marketNo certificate specifically references this device's Basic UDI-DI.