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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

MBAfp — Class I MDR by General Medical Merate…

MD Atlas
General Medical Merate S.p.A.

EUDAMED last updated this device on Nov 23, 2023

MBAfp

805489048TRDRE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: General Medical Merate S.p.A.
UDI-DI code: 08054890480727
Reference / catalog number: MBAfp

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View device family (Basic UDI)

Manufacturer information

Organization name: General Medical Merate S.p.A.
SRN: IT-MF-000023169
Manufacturer status: Active

Related devices

GE Medical Systems SCS805489048TLRRQOn the market GE Medical Systems SCS805489048TLRRQOn the market GE Medical Systems SCS805489048TLRRQOn the market GE Medical Systems SCS805489048TLRRQOn the market MBAep805489048TRDREOn 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: 08054890480727
Basic UDI-DI: 805489048TRDRE
Reference / catalog number: MBAfp
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: Fixed height stretcher with floating tabletop
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 200 MU10
95 MU29

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08054890480727

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V0899MEDICAL SUPPORT EQUIPMENT - 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.