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Aesculap AG devices, product family

by Aesculap AG 14 variants Basic UDI-DI 4039239000000309ZV

Shared by every variant

Manufacturer
Aesculap AG(14)
Basic UDI-DI
4039239000000309ZV
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 4039239000000309ZV.

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 4039239000000309ZV
UDI-DISize and differences
Aesculap DC094R04038653033881 —On the market
Aesculap DC200R04038653033898 —On the market
Aesculap DC227R04038653033966 —On the market
Aesculap DC228R04038653033973 —On the market
Aesculap DC239R04038653034000 —On the market
Aesculap DC241R04038653034017 —On the market
Aesculap DC250R04038653034024 —On the market
Aesculap DC251R04038653034031 —On the market
Aesculap DC252R04038653034048 —On the market
AESCULAP DC229R DC229R / DC229R04038653033980 —On the market
AESCULAP DC253R DC253R / DC253R04038653034055 —On the market
ERGOFILL DC471R04046955082278 —On the market
ERGOFILL DC475R04046955082285 —On the market
ERGOFILL DC479R04046955082292 —On the market