RoweWithdrawalStraw

Organization name

RoweMed AG - Medical 4 Life

SRN

DE-MF-000005350

Manufacturer status

Active

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

• CW009

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

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW001

  EUDAMED did not publish a description for this code.
• CW032

  EUDAMED did not publish a description for this code.
• CW999

  Exclusion of liability: if reprocessed for reuse, the physical, chemical and/or biological product properties may be changed
• CW999

  This product does not replace the required hygienic and aseptic working practices. Care must be taken to avoid contamination.
• CW999

  If the product is damaged or dropped, do not use it.
• CW999

  No liquid may be injected back into the ampoule.

Primary placement in Germany; available across 1 country total.

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

Trade name

RoweWithdrawalStraw

UDI-DI code

04250347602597

Basic UDI-DI

42503476ENTNAHMEHALMM2

Reference / catalog number

A-1312

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on 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.

• A0704SYSTEMS FOR RECONSTITUTION AND ADMINISTRATION OF PHARMACEUTICALS

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