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

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Organization name
UDI-DI code
Reference / catalog number

S-Haube-38B — Class I MDR by GVB-geliMED GmbH

MD Atlas
GVB-geliMED GmbH

EUDAMED last updated this device on Feb 7, 2025

S-Haube-38B

40491790001MU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GVB-geliMED GmbH
UDI-DI code: 04049179001513
Reference / catalog number: S-Haube-38B

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Manufacturer information

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

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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: 04049179001513
Basic UDI-DI: 40491790001MU
Reference / catalog number: S-Haube-38B
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: Wiederverwendbare EEG-Haube Schröter Silikon Größe 38 blau
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.