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Aesculap AG devices, product family

by Aesculap AG 17 variants Basic UDI-DI 4039239000000430ZR

Shared by every variant

Manufacturer
Aesculap AG(17)
Basic UDI-DI
4039239000000430ZR
Risk class
Class I
Legislation
MDR
EMDN category
ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER
Market status
17 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 4039239000000430ZR.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 17 devices listed on this page; other pages of the family can carry others.

Variants

17 devices · page 1 of 1

Variants of Aesculap AG devices, Basic UDI-DI 4039239000000430ZR
UDI-DISize and differences
PROSPACE SJ217R04046963775544 —On the market
PROSPACE SJ218R04046963775551 —On the market
PROSPACE SJ219R04046963775568 —On the market
PROSPACE SJ220R04046963775575 —On the market
PROSPACE SJ222R04046963775599 —On the market
PROSPACE SJ223R04046963775605 —On the market
TSPACE FJ647R04038653453009 —On the market
TSPACE FJ648R04038653453016 —On the market
TSPACE FJ649R04038653453023 —On the market
TSPACE FJ650R04038653453030 —On the market
TSPACE FJ651R04038653453047 —On the market
TSPACE FJ652R04038653453054 —On the market
TSPACE FJ653R04038653453061 —On the market
TSPACE FJ654R04038653453078 —On the market
TSPACE FJ655R04038653453085 —On the market
TSPACE FJ656R04038653453092 —On the market
TSPACE FJ657R04038653453108 —On the market