Organization name

Philips Ultrasound LLC

SRN

US-MF-000002237

Manufacturer status

Active

Primary placement in Germany; available across 32 countries total.

Trade name

Transducer C8-4v, Variant 5

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.

00884838067486

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.

0884838BM428T4

Reference / catalog number

989605368833

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

1

Additional product description

Diagnostic ultrasound imaging and fluid flow analysis of the human body

Additional information URL

https://www.usa.philips.com/healthcare/support/resource-center/results?sort=relevancy&f:@ps_contenttype=%5bInstruction%20for%20Use%5d&f:@ps_language=%5bEnglish%20%28US%29%2cEnglish%5d&f:@ps_modality=%5bUltrasound%5d

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.

• Z110402010201CURVILINEAR TRANSCUTANEOUS TWO–DIMENSIONAL ULTRASOUND PROBES (CONVEX–ARRAY)

• Class IIa medical devices in EUDAMED

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