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Aesculap AG devices, product family

by Aesculap AG 9 variants Basic UDI-DI 4039239000000317ZU

Shared by every variant

Manufacturer
Aesculap AG(9)
Basic UDI-DI
4039239000000317ZU
Risk class
Class I
Legislation
MDR
EMDN category
SELF-STATIC SPREADERS, REUSABLE
Market status
9 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 4039239000000317ZU.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 9 devices listed on this page; other pages of the family can carry others.

Variants

9 devices · page 1 of 1

Variants of Aesculap AG devices, Basic UDI-DI 4039239000000317ZU
UDI-DISize and differences
Aesculap TE749R04038653197248 —On the market
AESCULAP BW010R BW010R / BW010R04038653222827 —On the market
CCR BW047R04038653302130 —On the market
CCR BW048R04038653302147 —On the market
CCR BW049R04038653254873 —On the market
CCR-XX BW137R04046963397913 —On the market
CCR-XX BW138R04046963397920 —On the market
CCR-XX BW139R04046963397944 —On the market
CLR BW001R04038653222803 —On the market