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Aesculap, product family

by Aesculap AG 12 variants Basic UDI-DI 40392390000003942H

Shared by every variant

Manufacturer
Aesculap AG(12)
Basic UDI-DI
40392390000003942H
Risk class
Class I
Legislation
MDR
EMDN category
CRANIAL SURGERY SPREADERS AND RETRACTORS, REUSABLE - OTHERNERVES AND VESSELS HOOK RETRACTORS, REUSABLECEREBRAL SPREADERS AND RETRACTORS, REUSABLECLINICAL USE TRAYS AND BOWLS
Market status
12 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000003942H.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 12 devices listed on this page; other pages of the family can carry others.

Variants

12 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 40392390000003942H
UDI-DISize and differences
Aesculap FF161R04038653065271 —On the market
Aesculap FF163R04038653065288 —On the market
Aesculap FF165R04038653065295 —On the market
Aesculap FF180R04038653126873 —On the market
Aesculap FF266R04038653065356 —On the market
Aesculap FF270R04038653065387 —On the market
Aesculap FF273R04038653065394 —On the market
Aesculap FF274R04038653065400 —On the market
Aesculap FF282R04038653065431 —On the market
Aesculap FF283R04038653065448 —On the market
Aesculap FF284R04038653065455 —On the market
Aesculap FF431R04038653065554 —On the market