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Aesculap, product family

by Aesculap AG 6 variants Basic UDI-DI 40392390000004392E

Shared by every variant

Manufacturer
Aesculap AG(6)
Basic UDI-DI
40392390000004392E
Risk class
Class I
Legislation
MDR
EMDN category
UTERINE SURGICAL PROBES, REUSABLE
Market status
6 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000004392E.

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, Basic UDI-DI 40392390000004392E
UDI-DISize and differences
Aesculap EO010R04038653041268 —On the market
Aesculap EO012R04038653041275 —On the market
Aesculap EO013R04038653041282 —On the market
Aesculap EO015R04038653041299 —On the market
AESCULAP EO005R EO005R / EO005R04038653041251 —On the market
AESCULAP EO020 EO020 / EO02004038653041312 —On the market