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

M-T-LMEP-2737-18 — Class I MDR by GVB-geliMED GmbH

MD Atlas
GVB-geliMED GmbH

EUDAMED last updated this device on Aug 12, 2025

M-T-LMEP-2737-18

40491790001MU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GVB-geliMED GmbH
UDI-DI code: 04049179000301
Reference / catalog number: M-T-LMEP-2737-18

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: GVB-geliMED GmbH
SRN: DE-MF-000005314
Manufacturer status: Active

Related devices

003-6-00640491790001MUOn the market M-3-L40491790001MUOn the market M-3-S40491790001MUOn the market M-3-SI40491790001MUOn the market 003-0-70640491790001MUOn 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: 04049179000301
Basic UDI-DI: 40491790001MU
Reference / catalog number: M-T-LMEP-2737-18
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: MultiCap-Flat 51-57cm 27 Elektroden blau/rot
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

N01010203EEG HEADSETS

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.