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Aesculap AG devices, product family

by Aesculap AG 14 variants Basic UDI-DI 403923900000054024

Shared by every variant

Manufacturer
Aesculap AG(14)
Basic UDI-DI
403923900000054024
Risk class
Class I
Legislation
MDR
Market status
14 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 403923900000054024.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 14 devices listed on this page; other pages of the family can carry others.

Variants

14 devices · page 1 of 1

Variants of Aesculap AG devices, Basic UDI-DI 403923900000054024
UDI-DISize and differences
Aesculap DP150R04038653037957 —On the market
Aesculap DP151R04038653037964 —On the market
Aesculap DP152R04038653350698 —On the market
Aesculap DR780R04038653038435 —On the market
ERGOPERIO DX060R04046964540073 —On the market
ERGOPERIO DX061R04046964540080 —On the market
ERGOPERIO DX070R04046964540097 —On the market
ERGOPERIO DX071R04046964540103 —On the market
ERGOPERIO DX080R04046964540110 —On the market
ERGOPERIO DX081R04046964540127 —On the market
ERGOPLANT DX050R04038653385690 —On the market
ERGOPLANT DX051R04038653385713 —On the market
ERGOPLANT DX052R04038653385706 —On the market
ERGOPLANT DX055R04038653385720 —On the market