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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

5005006 — Class IIb MDD by AGOMED Medizin-Technik…

MD Atlas
AGOMED Medizin-Technik GmbH

EUDAMED last updated this device on Oct 18, 2023

5005006

B-04251576915588

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: AGOMED Medizin-Technik GmbH
UDI-DI code: 04251576915588
Reference / catalog number: 5005006

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Manufacturer information

Organization name: AGOMED Medizin-Technik GmbH
SRN: DE-MF-000013801
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
See IFU

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Aug 1, 2018	Still on market
Spain	Aug 1, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251576915588
Basic UDI-DI: B-04251576915588
Reference / catalog number: 5005006
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: TITANIUM SCREW 2,3 X 6 MM CANNULATED, PARTIAL THREAD, TX 6, PACK/1
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P09120603CANNULATED SCREWS

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

5005008B-04251576915595On 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.