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Aesculap, product family

by Aesculap AG 7 variants Basic UDI-DI 40392390000004962S

Shared by every variant

Manufacturer
Aesculap AG(7)
Basic UDI-DI
40392390000004962S
Risk class
Class I
Legislation
MDR
EMDN category
COSTOTOMES, REUSABLE
Market status
7 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000004962S.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 7 devices listed on this page; other pages of the family can carry others.

Variants

7 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 40392390000004962S
UDI-DISize and differences
Aesculap FB870R04038653158348 —On the market
Aesculap FB873R04038653158362 —On the market
Aesculap FB881R04038653158393 —On the market
Aesculap FB882R04038653158409 —On the market
Aesculap FB890R04038653158423 —On the market
AESCULAP FB878R FB878R / FB878R04038653158379 —On the market
AESCULAP FB892R FB892R / FB892R04038653158430 —On the market