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Aesculap AG devices, product family

by Aesculap AG 13 variants Basic UDI-DI 40392390000005442C

Shared by every variant

Manufacturer
Aesculap AG(13)
Basic UDI-DI
40392390000005442C
Risk class
Class IIa
Legislation
MDR
EMDN category
ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER
Market status
13 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000005442C.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 13 devices listed on this page; other pages of the family can carry others.

Variants

13 devices · page 1 of 1

Variants of Aesculap AG devices, Basic UDI-DI 40392390000005442C
UDI-DISize and differences
ABC FJ822R04038653200825 —On the market
ABC FJ823R04038653200832 —On the market
ABC FJ828R04038653200887 —On the market
ABC FJ834R04038653253074 —On the market
ABC FJ840R04038653327201 —On the market
ABC FJ845R04038653397006 —On the market
ABC FJ846R04038653377572 —On the market
ABC FJ896R04038653422883 —On the market
ABC FJ897R04038653422890 —On the market
ABC E-PLATE FJ837R04038653304899 —On the market
ABC2 FJ890R04038653405596 —On the market
ABC2 FJ910R04038653449934 —On the market
ABC2 FJ911R04038653449941 —On the market