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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

FSL210020 — Class I MDR by Pimp je Diabetes

MD Atlas
Pimp je Diabetes

EUDAMED last updated this device on Dec 11, 2025

FSL210020

8720865806TAPEFSL2FK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Pimp je Diabetes
UDI-DI code: 08720865806020
Reference / catalog number: FSL210020

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View device family (Basic UDI)

Manufacturer information

Organization name: Pimp je Diabetes
SRN: NL-MF-000033068
Manufacturer status: Active

Related devices

FSL2310308720865806TAPEFSL2FKOn the market FSL2300008720865806TAPEFSL2FKOn the market FSL2300108720865806TAPEFSL2FKOn the market FSL2300208720865806TAPEFSL2FKOn the market FSL2300308720865806TAPEFSL2FKOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08720865806020
Basic UDI-DI: 8720865806TAPEFSL2FK
Reference / catalog number: FSL210020
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: 2
Additional product description: Fixeer Tape t.b.v. Freestyle Libre 2 - Rond - Effen - Geel - 5 cm x 5 cm - 2 stuks
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

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

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