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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

13420201 — Class I MDR by Van Straten Medical B.V.

MD Atlas
Van Straten Medical B.V.

EUDAMED last updated this device on May 20, 2026

13420201

871841512143FG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Van Straten Medical B.V.
UDI-DI code: 08718415998622
Reference / catalog number: 13420201

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View device family (Basic UDI)

Manufacturer information

Organization name: Van Straten Medical B.V.
SRN: NL-MF-000002063
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		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08718415998622
Basic UDI-DI: 871841512143FG
Reference / catalog number: 13420201
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: Instrument basket 480x250x60 mm, equipped on the short side with a fixed flushing block with 10 openings, and 2 flushing holes on each long side of the basket.
Additional information URL: https://www.vanstratenmedical.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08718415998622

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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.

S010401TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS

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

CD HORIZON™ SOLERA™ 5.5/6.0 SPINAL SYSTEM STANDARD INSTRUMENTS BASKET 1 OF 3871841549-0000V9On the market GC-01-018718415GC-J-01FMOn the market Lid 360x250 mm871841549-0000V9On the market Lid 480x250 mm871841549-0000V9On the market Sterilisation basket with fixation for Dermatome 36x25x6cm871841549-0000V9On 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.