M1000

Organization name

Vircell, S.L

SRN

ES-MF-000004099

Manufacturer status

Active

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

• CW041

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW044

  EUDAMED did not publish a description for this code.

Primary placement in Spain; available across 32 countries total.

Trade name

not provided

UDI-DI code

08436040320280

Basic UDI-DI

B-08436040320280

Reference / catalog number

M1000

Issuing entity

GS1

Risk category

IVDD — General

Applicable legislation

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

Indirect immunoenzyme assay to test IgM antibodies against Legionella pneumophila serogroup 1 in human serum/plasma. The test is a qualitative and manual or alternatively automated assay, intended to be used as an aid to diagnosis.

Additional information URL

https://www.vircell.com/

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• W0105010502LEGIONELLA ANTIBODY ASSAYS

Certificate health across this manufacturer's portfolio.