ImmunoCAP IgE/ECP/Tryptase Sample Diluent

Organization name

Phadia AB

SRN

SE-MF-000014170

Manufacturer status

Active

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

• CW167

  EUDAMED did not publish a description for this code.
• CW166

  EUDAMED did not publish a description for this code.
• CW106

  EUDAMED did not publish a description for this code.
• CW083

  EUDAMED did not publish a description for this code.

Primary placement in Sweden; available across 31 countries total.

Trade name

ImmunoCAP IgE/ECP/Tryptase Sample Diluent

UDI-DI code

07333066016733

Basic UDI-DI

7333066BUDI0003LL

Reference / catalog number

10-9541-01

Issuing entity

GS1

Risk category

IVDR Class A

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

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.

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

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

• W01029003BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC)