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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

BIAPHASERTABS — Class I MDR by MEDI CAL HealthCare GmbH

MD Atlas
MEDI CAL HealthCare GmbH

EUDAMED last updated this device on Jan 23, 2026

BIAPHASERTABS

4260028553011S9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDI CAL HealthCare GmbH
UDI-DI code: 04260028550116
Reference / catalog number: 3011

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Manufacturer information

Organization name: MEDI CAL HealthCare GmbH
SRN: DE-MF-000018304
Manufacturer status: Active

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: BIAPHASERTABS
UDI-DI code: 04260028550116
Basic UDI-DI: 4260028553011S9
Reference / catalog number: 3011
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: 120
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)

C020501ECG ELECTRODES

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

Related devices

BIACLASSICTABS4260028553012SBOn the market BIACORPUS RX 4004M4260028553010S7On 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.