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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

16.536.13 P5G2 — Class I MDR by Kunststoffwerk…

MD Atlas
Kunststoffwerk Kremsmünster GmbH

EUDAMED last updated this device on May 8, 2026

16.536.13 P5G2

9008345MeasuringSpoonsTP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kunststoffwerk Kremsmünster GmbH
UDI-DI code: 09008345000151
Reference / catalog number: 16.536.13 P5G2

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View device family (Basic UDI)

Manufacturer information

Organization name: Kunststoffwerk Kremsmünster GmbH
SRN: AT-MF-000005252
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09008345000151
Basic UDI-DI: 9008345MeasuringSpoonsTP
Reference / catalog number: 16.536.13 P5G2
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: 4800
Additional product description: This medical device is intended for final placement on the market by pharmaceutical manufacturers together with a medicinal product. It is intended for the dosing and application of medicinal products until the medicinal product container is empty.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 1.25–5 MU48

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.

V0399MEASUREMENT DEVICES - 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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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.