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SP-GRIPFLOW, product family

by Fuji Systems Corporation, Shirakawa Plant 6 variants Basic UDI-DI 45440501910LM

Shared by every variant

Manufacturer
Fuji Systems Corporation, Shirakawa Plant(6)
Basic UDI-DI
45440501910LM
Risk class
Class III
Legislation
MDR
EMDN category
SELECTIVE CAROTID ARTERY AND CORONARY SINUS PERFUSION CANNULAS
Market status
6 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 45440501910LM.

Certificates

1 certificate naming this Basic UDI-DI · EUDAMED

  • MDR 810807 Technical documentation · refdata.applicable-legislation.mdr issued
    Notified body 2797 · holder Fuji Systems Corporation, Shirakawa Plant · issued 14 May 2026 · expires 13 May 2031

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 6 devices listed on this page; other pages of the family can carry others.

Variants

6 devices · page 1 of 1

Variants of SP-GRIPFLOW, Basic UDI-DI 45440501910LM
UDI-DISize and differences
SP-GRIPFLOW 1182212 / TYPE I, 12FR04544050125925 —On the market
SP-GRIPFLOW 1182214 / TYPE I, 12FR04544050125932 —On the market
SP-GRIPFLOW 1182216 / TYPE I, 12FR04544050125949 —On the market
SP-GRIPFLOW 1182312 / TYPE I, 12FR04544050125956 —On the market
SP-GRIPFLOW 1182314 / TYPE I, 12FR04544050125963 —On the market
SP-GRIPFLOW 1182316 / TYPE I, 12FR04544050125970 —On the market