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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

HandyHold Medium — Class I MDR by HandyLegs B.V.

MD Atlas
HandyLegs B.V.

EUDAMED last updated this device on Mar 31, 2026

HandyHold Medium

2866258HHV06B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HandyLegs B.V.
UDI-DI code: 08720892694034
Reference / catalog number: HandyHold Medium

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View device family (Basic UDI)

Manufacturer information

Organization name: HandyLegs B.V.
SRN: NL-MF-000023821
Manufacturer status: Active

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	Apr 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08720892694034
Basic UDI-DI: 2866258HHV06B
Reference / catalog number: HandyHold Medium
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: 1
Additional product description: Aantrek hulpmiddel voor therapeutisch elastische kousen
Additional information URL: https://handylegs.com/HandyHold
Clinical sizes: Medium

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720892694034

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

M030405COMPRESSION STOCKINGS

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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Related devices

HandyFix2866258HFV163On the market HandyFix2866258HFV2-XJOn the market HandyHold Extra extra large (XXL)2866258HHV06BOn the market HandyHold XL2866258HHV06BOn the market HandHold Large2866258HHV06BOn 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.