Organization name

Salter Labs

SRN

US-MF-000007934

Manufacturer status

Active

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

• Single patient multiple use

  This is a single-patient multi-use product, reuse on more than one patient may cause a risk of cross-contamination.

Primary placement in Germany; available across 21 countries total.

Trade name

Inline water trap with self-sealing end cap.

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.

20607411001240

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.

0607411TF20017cO2Tubing56

Reference / catalog number

7000-0-25

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 IIa

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.

• R03010204OXYGEN ADMINISTRATION TUBINGS

• Class IIa medical devices in EUDAMED

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