Organization name

Synaptic Medical Corporation

SRN

US-MF-000025093

Manufacturer status

Active

Primary placement in Germany; available across 32 countries total.

Trade name

Navigo

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.

00850026677379

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.

B-00850026677379

Reference / catalog number

S08574LL

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 III

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

The Steerable Intracardiac Catheter Introducer Kit includes a sheath introducer, a dilator and a guide wire.

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.

• C019015CARDIAC TRANSSEPTAL PUNCTURE KITS

• Class III medical devices in EUDAMED

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