Skip to content

PLASMAFIT, product family

by Aesculap AG 14 variants Basic UDI-DI 40392390000003892Q

Shared by every variant

Manufacturer
Aesculap AG(14)
Basic UDI-DI
40392390000003892Q
Risk class
Class IClass IIa (varies)
Legislation
MDR
EMDN category
TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTSORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER
Market status
14 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000003892Q.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 14 devices listed on this page; other pages of the family can carry others.

Variants

14 devices · page 1 of 1

Variants of PLASMAFIT, Basic UDI-DI 40392390000003892Q
UDI-DISize and differences
PLASMAFIT NT154704046955350100 —On the market
PLASMAFIT NT396R04046964115981 —On the market
PLASMAFIT NT397R04046964098406 —On the market
PLASMAFIT NT398R04046964098413 —On the market
PLASMAFIT NT399R04046964098420 —On the market
PLASMAFIT NT401R04046964093463 —On the market
PLASMAFIT NT403R04046964093395 —On the market
PLASMAFIT NT405R04046964093500 —On the market
PLASMAFIT NT437R04046964093371 —On the market
PLASMAFIT NT635R04046964115974 —On the market
PLASMAFIT REVISION NT541R04046955311408 —On the market
PLASMAFIT REVISION NT575R04046955311422 —On the market
PLASMAFIT REVISION NT577R04046955311446 —On the market
PLASMAFIT REVISION NT581R04046955311460 —On the market