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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

34610 755 636 — Class I MDR by VARTA Microbattery GmbH

MD Atlas
VARTA Microbattery GmbH

EUDAMED last updated this device on May 23, 2025

34610 755 636

40437522464A

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VARTA Microbattery GmbH
UDI-DI code: 04043752441710
Reference / catalog number: 34610 755 636

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Manufacturer information

Organization name: VARTA Microbattery GmbH
SRN: DE-MF-000005968
Manufacturer status: Active

Related devices

3460021041640437522464AOn the market 3460799743640437522464AOn the market 3460099743640437522464AOn the market 3461099743640437522464AOn the market 34607 822 63640437522464AOn 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

2 warnings recorded — scroll inside the panel to see all entries.

CW135
EUDAMED did not publish a description for this code.
CW296
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Netherlands; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04043752441710
Basic UDI-DI: 40437522464A
Reference / catalog number: 34610 755 636
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: 6
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)

Y214580HEARING AIDS OR HEARING DEVICES - ACCESSORIES

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