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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

06470 — Class IIa MDR by TECNIMED s.r.l.

MD Atlas
TECNIMED s.r.l.

EUDAMED last updated this device on Mar 10, 2023

06470

8022386VF064067BZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TECNIMED s.r.l.
UDI-DI code: 08022386064720
Reference / catalog number: 06470

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Manufacturer information

Organization name: TECNIMED s.r.l.
SRN: IT-MF-000007598
Manufacturer status: Active

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060008022386EDP01526063RBOn the market 064708022386VF064067BZOn the market 063008022386EDP01526063RBOn the market 052008022386EDP01526063RBOn the market 010008022386EDP01526063RBOn the market

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.
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		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08022386064720
Basic UDI-DI: 8022386VF064067BZ
Reference / catalog number: 06470
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
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.

V0301010202NON-CONTACT DIGITAL THERMOMETERS
V03010199THERMOMETERS - 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.