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Organization name
UDI-DI code
Reference / catalog number

UNI-TER STUART CLR — Class I MDD by Meus S.r.l.

MD Atlas
Meus S.r.l.

EUDAMED last updated this device on Feb 27, 2026

UNI-TER STUART CLR

B-08053848991650

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Meus S.r.l.
UDI-DI code: 08053848991650
Reference / catalog number: 230117

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View device family (Basic UDI)

Manufacturer information

Organization name: Meus S.r.l.
SRN: IT-MF-000021269
Manufacturer status: Active

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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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jan 1, 2000	Still on market

Device identification

Trade name: UNI-TER STUART CLR
UDI-DI code: 08053848991650
Basic UDI-DI: B-08053848991650
Reference / catalog number: 230117
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Plastic stick swab in PP test tube with stuart clear transport medium. Individually wrapped sterile .
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.

A1102SAMPLE COLLECTION SWABS WITH TRANSPORT MEDIUM

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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