- Role
- Country
- Date of registration
- Address
DE-MF-000005057Keil Skinfoam blau 30x30x31/1 cm 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 Jan 19, 2026
4001363PFLH001B7Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04001363008708
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 | Jul 17, 2024 | Still on market |
| Austria | Jul 17, 2024 | Still on market |
| Belgium | Jul 17, 2024 | Still on market |
| Denmark | Jul 17, 2024 | Still on market |
| Spain | Jul 17, 2024 | Still on market |
| France | Jul 17, 2024 | Still on market |
| Italy | Jul 17, 2024 | Still on market |
| Netherlands | Jul 17, 2024 | Still on market |
| Poland | Jul 17, 2024 | Still on market |
| Türkiye | Jul 17, 2024 | 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.
04001363008708Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4001363PFLH001B7153053UDI 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 marketKeil Skinfoam blau 28x18x9 cm4001363PFLH001B7On the marketKeil Skinfoam blau 30x30x15/1 cm4001363PFLH001B7On the marketKeil Skinfoam blau 34x38x25 cm4001363PFLH001B7On the marketKeil Skinfoam blau 36x24x7/1cm4001363PFLH001B7On the marketKeil Skinfoam blau 45x115x55/10 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.