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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

F-90R — Class IIa MDD by FAZZINI SRL

MD Atlas
FAZZINI SRL

EUDAMED last updated this device on May 15, 2026

F-90R

B-08051887991686

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: FAZZINI SRL
UDI-DI code: 08051887991686
Reference / catalog number: F-90R

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View device family (Basic UDI)

Manufacturer information

Organization name: FAZZINI SRL
SRN: IT-MF-000035989
Manufacturer status: Active

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F-205B-08051887991761On the market F-210 PROB-08051887991778On the market I.V. STAND805188799DT003E5On the market I.V. STAND805188799DT003E5On the market I.V. STAND805188799DT003E5On the market

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		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08051887991686
Basic UDI-DI: B-08051887991686
Reference / catalog number: F-90R
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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

UDI-DI DataMatrix

Encoded

(01)08051887991686

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EMDN nomenclature code(s)

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

Z120105SURGICAL MEDICAL ASPIRATORS

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.