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Aesculap, product family

by Aesculap AG 15 variants Basic UDI-DI 40392390000007412G

Shared by every variant

Manufacturer
Aesculap AG(15)
Basic UDI-DI
40392390000007412G
Risk class
Class I
Legislation
MDR
Market status
15 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000007412G.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 15 devices listed on this page; other pages of the family can carry others.

Variants

15 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 40392390000007412G
UDI-DISize and differences
Aesculap OG351R04038653176977 —On the market
Aesculap OG352R04038653051755 —On the market
Aesculap OG353R04038653176984 —On the market
Aesculap OG354R04038653207374 —On the market
Aesculap OG355R04038653176991 —On the market
Aesculap OG357R04046964072802 —On the market
Aesculap OK560R04046964093272 —On the market
Aesculap OK561R04046964093296 —On the market
Aesculap OK562R04046964093289 —On the market
Aesculap OP310R04038653180448 —On the market
Aesculap OP311R04038653180455 —On the market
Aesculap OP312R04038653180462 —On the market
Aesculap OP313R04038653180479 —On the market
AESCULAP OG350R OG350R / OG350R04038653051748 —On the market
AESCULAP OG356R OG356R / OG356R04046964072772 —On the market