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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

Mixing Pad, non-slip — Class I MDR by M. G. Kurth GmbH

MD Atlas
M. G. Kurth GmbH

EUDAMED last updated this device on May 22, 2026

Mixing Pad, non-slip

++G086AnmischblocksDJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: M. G. Kurth GmbH
UDI-DI code: ++G086809621
Reference / catalog number: 80962

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View device family (Basic UDI)

Manufacturer information

Organization name: M. G. Kurth GmbH
SRN: DE-MF-000045501
Manufacturer status: Active

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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

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Mixing Pad, non-slip
UDI-DI code: ++G086809621
Basic UDI-DI: ++G086AnmischblocksDJ
Reference / catalog number: 80962
Issuing entity: HIBCC

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 500
Additional product description: —
Additional information URL: https://www.mgk-kurth.com/ifu/
Clinical sizes: 12 MU10
20 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

++G086809621

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q010503IMPRESSION MATERIAL TRAYS, SINGLE-USE

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

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