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Aesculap AG devices, product family

by Aesculap AG 6 variants Basic UDI-DI 40392390000003862J

Shared by every variant

Manufacturer
Aesculap AG(6)
Basic UDI-DI
40392390000003862J
Risk class
Class I
Legislation
MDR
EMDN category
ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY 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 40392390000003862J.

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 AG devices, Basic UDI-DI 40392390000003862J
UDI-DISize and differences
Aesculap NG53304038653116560 —On the market
Aesculap NG53404038653116577 —On the market
Aesculap NG53504046964725463 —On the market
PLASMACUP DC NG48904046963743802 —On the market
PLASMACUP SC NG400 NG400 / NG40004038653116256 —On the market
PLASMACUP SC NG403 NG403 / NG40304038653116287 —On the market