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Aesculap, product family

by Aesculap AGand 1 other manufacturer record 6 variants Basic UDI-DI 40392390000006522G

Shared by every variant

Manufacturer
Aesculap AG(4)AESCULAP, INC.(2)
Several manufacturer records share this Basic UDI-DI.
Basic UDI-DI
40392390000006522G
Risk class
Class I
Legislation
MDR
EMDN category
SUTURE INSTRUMENTS, REUSABLE - OTHER
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 40392390000006522G.

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 40392390000006522G
UDI-DISize and differences
Aesculap
Aesculap AG
EF168R04038653151790 —On the market
Aesculap
Aesculap AG
PL152R04046964668708 —On the market
Aesculap
Aesculap AG
PL651R04038653181414 —On the market
Aesculap
Aesculap AG
PO193R04038653287369 —On the market
AESCULAP BM950R
AESCULAP, INC.
BM950R / BM950R04038653140466 —On the market
AESCULAP PL153R
AESCULAP, INC.
PL153R / PL153R04046964668715 —On the market