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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

Varex Imaging — Class IIb MDR by Varex Imaging Group…

MD Atlas
Varex Imaging Group Nederland B.V.

EUDAMED last updated this device on Apr 13, 2026

Varex Imaging

8718755006DS

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Varex Imaging Group Nederland B.V.
UDI-DI code: 08718755003789
Reference / catalog number: 168371

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View device family (Basic UDI)

Manufacturer information

Organization name: Varex Imaging Group Nederland B.V.
SRN: NL-MF-000002153
Manufacturer status: Active

Related devices

Varex ImagingB-08718755002959On the market Varex ImagingB-08718755002942On the market Varex ImagingB-08718755002973On the market Varex ImagingB-08718755002966On the market Varex ImagingB-08718755002607On 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
see manual

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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: Varex Imaging
UDI-DI code: 08718755003789
Basic UDI-DI: 8718755006DS
Reference / catalog number: 168371
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: ICX1141D
Additional information URL: https://www.vareximaging.com/ifu/
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)08718755003789

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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.

Z11030599RADIOLOGY INSTRUMENTS - 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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