RU/KM-PROBE

Organization name

BEACMED S.R.L.

SRN

IT-MF-000023616

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW135

  EUDAMED did not publish a description for this code.
• CW014

  EUDAMED did not publish a description for this code.
• CW259

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 2 countries total.

Trade name

not provided

UDI-DI code

08059016710580

Basic UDI-DI

805901671KEATMENL6

Reference / catalog number

RU/KM-PROBE

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.

• U070399PELVIC FLOOR REHABILITATION DEVICES - OTHER