EDTA TUBE TRI-K R/BOT 2.5ML PP

Organization name

Deltalab, S.L.

SRN

ES-MF-000000153

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW010

  Avoid extreme temperatures. Do not use it if the product has changed its original color. Do not use if dirtiness is visible. Do not use if expiry date is exceeded. Do not use if broken or with missing components. Disposal as biological waste.

Primary placement in Spain; available across 2 countries total.

Trade name

EDTA TUBE TRI-K R/BOT 2.5ML PP

UDI-DI code

08435263850666

Basic UDI-DI

84356058UDI-DI-166D

Reference / catalog number

601603

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

12

Additional product description

—

Additional information URL

https://www.deltalabgroup.com/eifus

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.

• W0501010201CAPILLARY BLOOD COLLECTION SYSTEMS