- Role
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- Date of registration
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DE-MF-000005057Hinterkopfunterlage Skinfoam gelb is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by POLYFORM-Kunststofftechnik GmbH &Co. Betriebs KG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Dec 22, 2025
4001363PFLH001B7Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04001363001051
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 10 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Sep 10, 2020 | Still on market |
| Austria | Sep 10, 2020 | Still on market |
| Belgium | Sep 10, 2020 | Still on market |
| Denmark | Sep 10, 2020 | Still on market |
| Spain | Sep 10, 2020 | Still on market |
| France | Sep 10, 2020 | Still on market |
| Italy | Sep 10, 2020 | Still on market |
| Netherlands | Sep 10, 2020 | Still on market |
| Poland | Sep 10, 2020 | Still on market |
| Türkiye | Sep 10, 2020 | 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.
04001363001051Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4001363PFLH001B7107232UDI 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.
V080302PATIENT POSITIONING MEDICAL CUSHIONS4001363PFLH001B7On the marketHinterkopfunterlage Skinfoam blau-grau 250x245x95 mm4001363PFLH001B7On the marketHinterkopfunterlage Skinfoam blau, 250x245x75mm4001363PFLH001B7On the marketHinterkopfunterlage Skinfoam gelb4001363PFLH001B7On the marketHinterkopfunterlage Skinfoam gelb 21,5x23x7 cm4001363PFLH001B7On the marketHinterkopfunterlage Skinfoam violett 215x230x70 mm4001363PFLH001B7On the marketNo 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.