Full Handle Backflush 23G Standard Active/Passive

Organization name

AKTIVE SRL

SRN

IT-MF-000007813

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW009

  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.
• CW032

  Do not use past indicated expiration date

Primary placement in Italy; available across 32 countries total.

Trade name

Full Handle Backflush 23G Standard Active/Passive

UDI-DI code

08052276026446

Basic UDI-DI

8052276FT0001ID3CC

Reference / catalog number

AK-0454/AP

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

6

Additional product description

Manipolo Backflush 23G Standard Attivo/Passivo

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 23 MU999

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

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

• Q021199OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER