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Aesculap, product family

by Aesculap AGand 1 other manufacturer record 7 variants Basic UDI-DI 40392390000004752J

Shared by every variant

Manufacturer
Aesculap AG(5)AESCULAP, INC.(2)
Several manufacturer records share this Basic UDI-DI.
Basic UDI-DI
40392390000004752J
Risk class
Class I
Legislation
MDR
EMDN category
NASAL AND PARANASAL CAVITY SURGERY PLIERS, REUSABLE
Market status
7 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000004752J.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 7 devices listed on this page; other pages of the family can carry others.

Variants

7 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 40392390000004752J
UDI-DISize and differences
Aesculap
Aesculap AG
OK711R04038653177561 —On the market
Aesculap
Aesculap AG
OK737R04038653177585 —On the market
Aesculap
Aesculap AG
OK741R04038653177608 —On the market
Aesculap
Aesculap AG
OK742R04038653177615 —On the market
Aesculap
Aesculap AG
OK745R04038653177639 —On the market
AESCULAP OK712R
AESCULAP, INC.
OK712R / OK712R04038653177578 —On the market
AESCULAP OK740R
AESCULAP, INC.
OK740R / OK740R04038653177592 —On the market