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Aesculap, product family

by Aesculap AGand 1 other manufacturer record 6 variants Basic UDI-DI 40392390000006502C

Shared by every variant

Manufacturer
Aesculap AG(5)AESCULAP, INC.(1)
Several manufacturer records share this Basic UDI-DI.
Basic UDI-DI
40392390000006502C
Risk class
Class IIaClass I (varies)
Legislation
MDR
EMDN category
ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER
Market status
5 on the market1 no longer on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000006502C.

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 40392390000006502C
UDI-DISize and differences
Aesculap
Aesculap AG
KY201R04038653174669 —On the market
Aesculap
Aesculap AG
KY203R04038653174683 —On the market
Aesculap
Aesculap AG
KY204R04038653174690 —On the market
Aesculap
Aesculap AG
KY205R04038653174706 —On the market
Aesculap
Aesculap AG
KY206R04038653174713 —On the market
AESCULAP KY202R
AESCULAP, INC.
KY202R / KY202R04038653174676 —No longer on the market