Organization name

Salter Labs

SRN

US-MF-000007934

Manufacturer status

Active

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

• Single patient multiple use
• Do not sterilise

Primary placement in Germany; available across 21 countries total.

Trade name

Filter

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.

00607411000980

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.

0607411TF20010_SleepDx9V

Reference / catalog number

1001-0-25

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 I

Applicable legislation

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

Status

On the market

Quantity

25

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.

• Z12100585POLYSOMNOGRAPHY INSTRUMENTS - CONSUMABLES

• Class I medical devices in EUDAMED

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