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Aesculap, product family

by Aesculap AG 6 variants Basic UDI-DI 403923900000069736

Shared by every variant

Manufacturer
Aesculap AG(6)
Basic UDI-DI
403923900000069736
Risk class
Class I
Legislation
MDR
EMDN category
ADENOTOMES, 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 403923900000069736.

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 403923900000069736
UDI-DISize and differences
Aesculap OM391R04038653469291 —On the market
Aesculap OM392R04038653469307 —On the market
Aesculap OM393R04038653469314 —On the market
Aesculap OM396R04038653469321 —On the market
Aesculap OM397R04038653469338 —On the market
Aesculap OM398R04038653469345 —On the market