Aesculap, product family

Manufacturer

Aesculap AG(15)·AESCULAP, INC.(1)

Several manufacturer records share this Basic UDI-DI.

Basic UDI-DI

403923900000033623

Risk class

Class I

Legislation

MDR

EMDN category

ENT INSTRUMENTS, REUSABLE - OTHER·GENERAL SURGERY DISSECTORS, REUSABLE·VASCULAR SPATULAS, REUSABLE·ORTHOPAEDIC SURGERY RASPS, REUSABLE·NEUROSURGERY SPATULAS AND DISSECTORS, REUSABLE

Market status

16 on the market

Official record

EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 403923900000033623.

No recall matched the devices on this page.

Recalls matched to the 16 devices listed on this page; other pages of the family can carry others.