M040PL

Organization name

Serrix B.V

SRN

NL-MF-000005882

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW275

  When pregnant or breastfeeding, only use if instructed by and under supervision of a health care professional
• CW010

  Consult instruction for use (symbol)
• CW262

  Single patient, multiple use (symbol)

Primary placement in Poland; available across 1 country total.

Trade name

not provided

UDI-DI code

08718309702656

Basic UDI-DI

871830970M0X0EGC8

Reference / catalog number

M040PL

Issuing entity

GS1

Risk category

Class IIa

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.

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

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

• V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER