Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

XD022011LEDER — Class I MDR by Moltoplast GmbH

MD Atlas
Moltoplast GmbH

EUDAMED last updated this device on Mar 17, 2026

XD022011LEDER

9006018DFLAP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Moltoplast GmbH
UDI-DI code: 90060182403238
Reference / catalog number: XD022011LEDER

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Moltoplast GmbH
SRN: AT-MF-000004503
Manufacturer status: Active

Related devices

XTEVACMAT9006018MOEVACTDOn the market MAPFFAVUSANEVACTWIN1509006018MAPFXHOn the market 63903025019006018MAPFXHOn the market 63902029019006018MAPFXHOn the market MAPFFAVUSANPUNLSILVER4809006018MAPFXHOn the market

Certificates

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.

Market distribution

Primary placement in Austria; available across 3 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Germany		Still on market
Italy		Still on market

Device identification

Trade name: not provided
UDI-DI code: 90060182403238
Basic UDI-DI: 9006018DFLAP
Reference / catalog number: XD022011LEDER
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Keilkissen MPF® L500xA400xB120/C40 Kunstleder W
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONS
V080302PATIENT POSITIONING MEDICAL CUSHIONS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification