Organization name

CIVCO Medical Instruments Co., Inc. dba CIVCO and CIVCO Medical Solutions

SRN

US-MF-000008229

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 32 countries total.

Trade name

Ultrasound Pad

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

00841436114967

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

0841436101TD201B2NP

Reference / catalog number

H2O-007

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIa

Applicable legislation

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

Status

On the market

Quantity

100

Additional product description

Non-sterile (8.25 x x12.7cm) hydrophilic ultrasound pad with adhesive

Additional information URL

https://www.civco.com/

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.

• T030102COVER SHEATHS, INSTRUMENTS AND EQUIPMENTS

• Class IIa medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.