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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

9681ML — Class I MDR by Lurvink Corporate B.V.

MD Atlas
Lurvink Corporate B.V.

EUDAMED last updated this device on Sep 26, 2024

9681ML

8717882CG.BlueCareMS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lurvink Corporate B.V.
UDI-DI code: 08717882321025
Reference / catalog number: 9681ML

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View device family (Basic UDI)

Manufacturer information

Organization name: Lurvink Corporate B.V.
SRN: NL-MF-000044152
Manufacturer status: Active

Related devices

9681MS8717882CG.BlueCareMSOn the market 9682MS8717882CG.BlueCareMSOn the market 9682ML8717882CG.BlueCareMSOn the market 9681MM 8717882CG.BlueCareMSOn the market 9682MM 8717882CG.BlueCareMSOn 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.

CW009
For single use only.

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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: 08717882321025
Basic UDI-DI: 8717882CG.BlueCareMS
Reference / catalog number: 9681ML
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: 100
Additional product description: —
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

EMDN nomenclature code(s)

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

T01020204NITRILE EXAMINATION / TREATMENT GLOVES

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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