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

8099093 — Class I MDR by Meyra GmbH

MD Atlas
Meyra GmbH

EUDAMED last updated this device on Apr 27, 2026

8099093

4032766347458L

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Meyra GmbH
UDI-DI code: 04032766357391
Reference / catalog number: 8099093

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: Meyra GmbH
SRN: DE-MF-000005780
Manufacturer status: Active

Related devices

1.73640327662379189On the market 9173604640327662379189On the market 9173604240327662379189On the market 1.73640327662379189On the market 1.73540327662645387On 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04032766357391
Basic UDI-DI: 4032766347458L
Reference / catalog number: 8099093
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: Die Finger- bzw. Formschiene dient in erster Linie der Fixierung eines Gelenkes bzw. einer Extremität zu dessen kurz- bis mittelfristigen Ruhigstellung bei Gelenk-, Knochen- und Weichteilverletzungen sowie degenerativen Veränderungen, Instabilität und entzündlichen Prozessen.
Additional information URL: https://www.meyra.de/reha-pflege-alltagshilfen/reha-und-alltag/reha-alltag-details/formschiene-24
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y241899ARM, HAND, FINGER FUNCTION AID AND/OR SUBSTITUTION DEVICES - OTHER

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