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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

13 10 30 — IVDR Class A IVDR by GP Medical Devices A/S

MD Atlas
GP Medical Devices A/S

EUDAMED last updated this device on Jan 28, 2025

13 10 30

5711276EasySamplerBASICX7

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: GP Medical Devices A/S
UDI-DI code: 05711276131309
Reference / catalog number: 13 10 30

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View device family (Basic UDI)

Manufacturer information

Organization name: GP Medical Devices A/S
SRN: DK-MF-000022391
Manufacturer status: Active

Related devices

20 25 005711276EasyDrainerNBOn the market 13 10 005711276EasySamplerBASICX7On the market 13 70 005711276EasySamplerBASICX7On the market 13 10 205711276EasySamplerBASICX7On the market 10 70 305711276EasySamplerEUEWOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05711276131309
Basic UDI-DI: 5711276EasySamplerBASICX7
Reference / catalog number: 13 10 30
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Flushable faeces collection paper for OEM customer with printed Instructions for Use and adhesive strips. 500 pcs. in a carton
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)05711276131309

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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.

W05019001FAECES COLLECTION DEVICES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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