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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

HEYRN86802S — Class IIa MDR by ITW LLC & Co. KG

MD Atlas
ITW LLC & Co. KG

EUDAMED last updated this device on Apr 28, 2026

HEYRN86802S

401911400MKKQ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ITW LLC & Co. KG
UDI-DI code: 04019114050616
Reference / catalog number: HEYRN86802S

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Manufacturer information

Organization name: ITW LLC & Co. KG
SRN: DE-MF-000006443
Manufacturer status: Active

Related devices

87505401911400MKKQOn the market 86804401911400MKKQOn the market ABELE867010S401911400MKKQOn the market ACUS86701S401911400MKKQOn the market ACUS86801S401911400MKKQOn the market

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Italy		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04019114050616
Basic UDI-DI: 401911400MKKQ
Reference / catalog number: HEYRN86802S
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
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)

D99DISINFECTANTS, ANTISEPTICS, STERILISING AGENTS AND DETERGENTS FOR MEDICAL DEVICES - OTHER

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.