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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

05BM591.01 — Class IIa MDD by Betamed Srl

MD Atlas
Betamed Srl

EUDAMED last updated this device on Feb 4, 2026

05BM591.01

B-08034139610009

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Betamed Srl
UDI-DI code: 08034139610009
Reference / catalog number: 05BM591.01

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View device family (Basic UDI)

Manufacturer information

Organization name: Betamed Srl
SRN: IT-MF-000034707
Manufacturer status: Active

Related devices

06BM601B-08034139610061On the market 05BMSPA.ARTB-08034139611747On the market 05BM591.02B-08034139610023On the market 05BMMANB-08034139611754On the market 05BM591.03B-08034139610047On the market

Critical warnings

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

CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

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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: 08034139610009
Basic UDI-DI: B-08034139610009
Reference / catalog number: 05BM591.01
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: KIT ISTEROSCOPIA
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.

T0202SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)

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.