Organization name

B. Braun Melsungen AG

SRN

DE-MF-000000201

Manufacturer status

Active

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

• Caution
• Do not use past indicated date
• Do not re-use
• Contains a medicinal substance
• Do not resterilize
• Do not use if package is damaged
• Consult instructions for use

Primary placement in Germany; available across 27 countries total.

Trade name

SeQuent®

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.

04046955924677

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.

40392390000013492K

Reference / catalog number

5023404

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

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

Status

On the market

Quantity

1

Additional product description

SEQUENT® PLEASE ASCEND 3.0X10MM

Additional information URL

https://eifu.bbraun.com/

Clinical sizes

• 10 MM
• 3 MM
• 14 BAR
• 145 CM

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

• 04046955924677× 1 unitBase unit
  • 04046955975952× 10 units

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

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

• C010401020199PTCA DIALATION CATHETERS - OTHER

• Class III medical devices in EUDAMED

• G70 012974 0637Amended
  Technical documentationNotified body: TÜV SÜD Product Service GmbH (0123)Expiry: Sep 6, 2028

Certificate health across this manufacturer's portfolio.