Organization name

FUJIFILM medwork GmbH

SRN

DE-MF-000008444

Manufacturer status

Active

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

• Consult instructions for use
• Do not re-use
• Do not resterilize
• Do not use if package is damaged
• Refer to instruction manual/booklet

Primary placement in Germany; available across 32 countries total.

Trade name

PRO1-S1-05-220-35

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.

04044503035240

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.

4044503056484K

Reference / catalog number

70100146829

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

1

Additional product description

—

Additional information URL

https://med-lib.fujifilm.com/

Clinical sizes

• 9 MU170

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

• 04044503035240× 1 unitBase unit
  • 14044503035247× 2 units

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

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

• G030499ERCP AND SPHINCTEROTOMY DEVICES - OTHER

• Class I medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.