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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

MUALEST01 — Class I MDR by Mesa Ideas SRL

MD Atlas
Mesa Ideas SRL

EUDAMED last updated this device on Mar 26, 2024

MUALEST01

805957138MUALEST00WZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mesa Ideas SRL
UDI-DI code: 08059571380051
Reference / catalog number: MUALEST01

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View device family (Basic UDI)

Manufacturer information

Organization name: Mesa Ideas SRL
SRN: IT-MF-000029839
Manufacturer status: Active

Related devices

Sagittarius 2023 / MUAAASA15805957138MUAAASA15NLOn the market MUAAASA15-M805957138MUAAASA15NLOn the market MISWBA00 - V. 0.9.15.0805957138MISWBA00E8On the market MISWBA00 - V. 0.9.17.0 Editor805957138MISWBA00E8On the market MISWBA00 - V. 0.9.14.0805957138MISWBA00E8On the market

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.

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

Device identification

Trade name: not provided
UDI-DI code: 08059571380051
Basic UDI-DI: 805957138MUALEST00WZ
Reference / catalog number: MUALEST01
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: Stativo da letto e poltrona con piedi fissi
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.

Y2499DEVICES FOR OBJECT MANIPULATION - 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.