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

202 210 - Dunkelgrau — Class I MDR by feela., Marco Winter,…

MD Atlas
feela., Marco Winter, e-Commerce

EUDAMED last updated this device on Jan 31, 2024

202 210 - Dunkelgrau

4744999462022X337

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: feela., Marco Winter, e-Commerce
UDI-DI code: 04744999460631
Reference / catalog number: 202 210 - Dunkelgrau

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: feela., Marco Winter, e-Commerce
SRN: DE-MF-000011263
Manufacturer status: Active

Related devices

Art. 201 804 - Dunkelgrau47449994620180X2HOn the market Art. 201 804 - Schwarz47449994620180X2HOn the market Art. 201 804 - Silber47449994620180X2HOn the market 202 209, 202 210, 202 2114744999462022X337On the market 202 209 - Dunkelgrau4744999462022X337On the market

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: 04744999460631
Basic UDI-DI: 4744999462022X337
Reference / catalog number: 202 210 - Dunkelgrau
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080399MEDICAL CUSHIONS - 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

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.