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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

08-2502 — Class I MDR by Linkfar Healthcare GmbH

MD Atlas
Linkfar Healthcare GmbH

EUDAMED last updated this device on Jul 9, 2025

08-2502

42700047795APWS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Linkfar Healthcare GmbH
UDI-DI code: 04270004779516
Reference / catalog number: 08-2502

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Manufacturer information

Organization name: Linkfar Healthcare GmbH
SRN: DE-MF-000042858
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Jul 9, 2025	Still on market
Italy	Jul 9, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04270004779516
Basic UDI-DI: 42700047795APWS
Reference / catalog number: 08-2502
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: 15
Additional product description: The CGM/Pump patch is a non-sterile, single-use adhesive patch intended for external use only. It is designed to assist in the fixation of continuous glucose monitoring (CGM) sensors or insulin pump components to the skin. The patch helps maintain the position of such devices during daily activities. This product is a non-essential accessory and does not affect the safety or performance of the primary medical device. It is not intended for diagnostic or therapeutic purposes and does not come into contact with open wounds or mucous membranes.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

H900299TAPES, MEDICAL/SURGICAL - 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

Related devices

08-250542700047795APWSOn the market 08-250342700047795APWSOn 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.