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Aesculap AG devices, product family

by Aesculap AG 6 variants Basic UDI-DI 4039239000000303ZH

Shared by every variant

Manufacturer
Aesculap AG(6)
Basic UDI-DI
4039239000000303ZH
Risk class
Class I
Legislation
MDR
EMDN category
ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHERORTHOPAEDIC SURGERY HAMMERS, REUSABLE
Market status
4 on the market2 no longer on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 4039239000000303ZH.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 6 devices listed on this page; other pages of the family can carry others.

Variants

6 devices · page 1 of 1

Variants of Aesculap AG devices, Basic UDI-DI 4039239000000303ZH
UDI-DISize and differences
A-SPACE SIBD SJ604R04046963669874 —On the market
A-SPACE SIBD SJ608R04046963670313 —On the market
A-SPACE SIBD SJ705R SJ705R / SJ705R04046963670504 —No longer on the market
Aesculap SJ709R04046963895587 —On the market
AESCULAP SJ708T SJ708T / SJ708T04046964061141 —No longer on the market
HYDROLIFT FW440R04046963408923 —On the market