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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

D1-700g — Class I MDR by MSK drevels

MD Atlas
MSK drevels

EUDAMED last updated this device on May 20, 2026

D1-700g

87208928861DR19H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MSK drevels
UDI-DI code: 08720892886132
Reference / catalog number: D1-700g

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View device family (Basic UDI)

Manufacturer information

Organization name: MSK drevels
SRN: NL-MF-000051666
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	Jan 15, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08720892886132
Basic UDI-DI: 87208928861DR19H
Reference / catalog number: D1-700g
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: Hulpmiddel dat door artsen en therapeuten wordt gebruikt om mechanische tikken op de huid boven gewrichten te geven ter ondersteuning bij musculoskeletale behandelingen. Een drevel is een niet-actief hulpmiddel dat wordt gebruikt in combinatie met een lichte zandhamer (niet geleverd door fabrikant). Het bestaat uit een aluminium handvat met RVS kern, met een rubberen dop die in contact komt met de huid van de patiënt.
Additional information URL: https://www.mskdrevels.nl/gebruiksaanwijzing
Clinical sizes: 700 MU24

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720892886132

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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.

Z12139080VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - HARDWARE ACCESSORIES

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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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.