Organization name

Aesculap AG

SRN

DE-MF-000005504

Manufacturer status

Active

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

Primary placement in Germany; available across 27 countries total.

Trade name

CESPACE

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.

04038653450077

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.

40392390000003842E

Reference / catalog number

FJ387R

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

CESPACE PEEK TRIAL IMPL.5° 14X7MM ANAT.

Additional information URL

https://eifu.bbraun.com/

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.

• L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER

• Class IIa medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.