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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

SU000 — Class IIa MDR by R.A.W. Srl

MD Atlas
R.A.W. Srl

EUDAMED last updated this device on Aug 21, 2025

SU000

8052141890004SU00H9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: R.A.W. Srl
UDI-DI code: 08052141890103
Reference / catalog number: SU000

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View device family (Basic UDI)

Manufacturer information

Organization name: R.A.W. Srl
SRN: IT-MF-000027589
Manufacturer status: Active

Related devices

ABFT0008052141890004ABFTEHOn the market EN0008052141890004ENDGG9On the market SIR0008052141890004SIR0JGOn the market MIR0008052141890004MIR0H6On the market MK0008052141890004MK00EDOn 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

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW999
Sterilized using ethylene oxide
CW999
Single sterile barrier system with protective packaging outside

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	Jul 31, 2023	Still on market
Spain	Jul 31, 2023	Sep 6, 2024

Device identification

Trade name: not provided
UDI-DI code: 08052141890103
Basic UDI-DI: 8052141890004SU00H9
Reference / catalog number: SU000
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: https://www.rawbiomed.com/download-center
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)08052141890103

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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.

Z12011480SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES

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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