Organization name

B. Braun Medical AG

SRN

CH-MF-000017781

Manufacturer status

Active

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

• H226 – Flammable liquid and vapour.
• H302 – Harmful if swallowed.
• H314 – Causes severe skin burns and eye damage.
• P301 – IF SWALLOWED: P330 – Rinse mouth.
• P301 – IF SWALLOWED: P331 – Do NOT induce vomiting.
• P305 – IF IN EYES: P338 – Remove contact lenses, if present and easy to do. Continue rinsing.
• P305 – IF IN EYES: P351 – Rinse cautiously with water for several minutes.
• P303 – IF ON SKIN (or hair): P353 – Rinse skin with water/shower.
• P303 – IF ON SKIN (or hair): P361 – Remove/Take off immediately all contaminated clothing.
• Do not use past indicated date
• P280 – Wear protective gloves/protective clothing/eye protection/face protection.
• P273 – Avoid release to the environment.
• P210 – Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
• H410 – Very toxic to aquatic life with long lasting effects.
• H372 – Causes damage to organs through prolonged or repeated exposure exposure cause the hazard>.

Primary placement in Germany; available across 27 countries total.

Trade name

Stabimed®

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.

07612449137150

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.

40392390000009112H

Reference / catalog number

19690

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

STABIMED FRESH CANISTER "WEST" 5LT

Additional information URL

https://eifu.bbraun.com/

Clinical sizes

• 5 L

1 packaging level registered — each level carries its own UDI-DI.

• 07612449137150× 1 unitBase unit
  • 07612449137167× 128 units

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• D0902ASSOCIATED AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES

• Class IIa medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

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