Skip to content

Aesculap AG devices, product family

by Aesculap AG 10 variants Basic UDI-DI 4039239000000301ZD

Shared by every variant

Manufacturer
Aesculap AG(10)
Basic UDI-DI
4039239000000301ZD
Risk class
Class I
Legislation
MDR
EMDN category
ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHEROSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHERORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE
Market status
10 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 4039239000000301ZD.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 10 devices listed on this page; other pages of the family can carry others.

Variants

10 devices · page 1 of 1

Variants of Aesculap AG devices, Basic UDI-DI 4039239000000301ZD
UDI-DISize and differences
A-SPACE SIBD SJ020R04046963081430 —On the market
A-SPACE SIBD SJ022R04046963081454 —On the market
A-SPACE SIBD SJ024R04046963081478 —On the market
A-SPACE SIBD SJ026R04046963081492 —On the market
A-SPACE SIBD SJ028R04046963081515 —On the market
A-SPACE SIBD SJ030R04046963081539 —On the market
Aesculap ME017R04046964093852 —On the market
Aesculap SJ725R04046963895808 —On the market
ARCADIUS XP L ME189R04046964828775 —On the market
ARCADIUS XP L ME190R04046964828768 —On the market