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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

013061XS — Class I MDR by CLINI-LAB SRL

MD Atlas
CLINI-LAB SRL

EUDAMED last updated this device on Mar 2, 2026

013061XS

8029686EXAMGLOVESTLB7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CLINI-LAB SRL
UDI-DI code: 88029686200083
Reference / catalog number: 013061XS

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View device family (Basic UDI)

Manufacturer information

Organization name: CLINI-LAB SRL
SRN: IT-MF-000007798
Manufacturer status: Active

Related devices

35906.1S8029686CLINIBAGST7JOn the market 013402.S8029686EXAMGLOVESTNBBOn the market 013402.M8029686EXAMGLOVESTNBBOn the market 013402.XS8029686EXAMGLOVESTNBBOn the market 013402.XL8029686EXAMGLOVESTNBBOn 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

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 88029686200083
Basic UDI-DI: 8029686EXAMGLOVESTLB7
Reference / catalog number: 013061XS
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: Powder-free latex gloves, sterile, in single pack
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.

T010201LATEX 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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