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Organization name
UDI-DI code
Reference / catalog number

MI1425180195 — Class I MDR by Manifattura Falomo S.r.l.

MD Atlas
Manifattura Falomo S.r.l.

EUDAMED last updated this device on May 14, 2026

MI1425180195

805360865MIUH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Manifattura Falomo S.r.l.
UDI-DI code: 08053608653903
Reference / catalog number: MI1425180195

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View device family (Basic UDI)

Manufacturer information

Organization name: Manifattura Falomo S.r.l.
SRN: IT-MF-000025751
Manufacturer status: Active

Related devices

MI1425080190805360865MIUHOn the market MI1425080195805360865MIUHOn the market MI1425080200805360865MIUHOn the market MI1425085190805360865MIUHOn the market MI1425085195805360865MIUHOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Nov 18, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08053608653903
Basic UDI-DI: 805360865MIUH
Reference / catalog number: MI1425180195
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: —
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.

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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