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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

VITRILOCK — IVDD — General IVDD by VITROMED GmbH

MD Atlas
VITROMED GmbH

EUDAMED last updated this device on Jun 7, 2024

VITRILOCK

B-04260531792782

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: VITROMED GmbH
UDI-DI code: 04260531792782
Reference / catalog number: BG-VLG-U

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Manufacturer information

Organization name: VITROMED GmbH
SRN: DE-MF-000005131
Manufacturer status: Active

Related devices

- V-CULTUREDISHB-04260531792263On the market - V-ROUNDTUBEB-04260531792348On the market - V-ROUNDTUBEB-04260531792362On the market V- CULTUREDISHB-04260531792287On the market V- CULTUREDISHB-04260531792300On 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

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

CW010
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: VITRILOCK
UDI-DI code: 04260531792782
Basic UDI-DI: B-04260531792782
Reference / catalog number: BG-VLG-U
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic 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.

EMDN nomenclature code(s)

U08020401CRYOPRESERVATION CONTAINERS/STRAWS/VIALS FOR ASSISTED REPRODUCTION

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification