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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

660400 — Class I MDR by The Surgical Company…

MD Atlas
The Surgical Company International B.V.

EUDAMED last updated this device on Feb 25, 2026

660400

8719867EMDNZ12030380AGHX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: The Surgical Company International B.V.
UDI-DI code: 18719867001639
Reference / catalog number: 660400

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View device family (Basic UDI)

Manufacturer information

Organization name: The Surgical Company International B.V.
SRN: NL-MF-000001973
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.

Placed on the market in Netherlands; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 18719867001639
Basic UDI-DI: 8719867EMDNZ12030380AGHX
Reference / catalog number: 660400
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: The Fluido® AirGuard detects air in the de-aeration chamber of the Fluido® Disposable Sets by means of an ultrasonic sensor.
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

UDI-DI DataMatrix

Encoded

(01)18719867001639

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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.

Z12030380INFUSION 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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650100B-18719867001554On the market 6607008719867EMDNV0899FCHJMOn the market 672000B-18719867001776On the market 650200B-18719867001561On the market 660200A8719867EMDNZ12030380CQWOn 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.