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ENDOTRACHEAL, product family

by Romsons Group Private Limited 8 variants Basic UDI-DI 8902120B001RF

Shared by every variant

Basic UDI-DI
8902120B001RF
Risk class
Class IIa
Legislation
MDR
Market status
8 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 8902120B001RF.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 8 devices listed on this page; other pages of the family can carry others.

Variants

8 devices · page 1 of 1

Variants of ENDOTRACHEAL, Basic UDI-DI 8902120B001RF
UDI-DISize and differences
ENDOTRACHEAL TUBE CUFFED GS-200408907265200461 —On the market
ENDOTRACHEAL TUBE CUFFED GS-200408907265200485 —On the market
ENDOTRACHEAL TUBE-CUFFED GS-200408902120200457 —On the market
ENDOTRACHEAL TUBE-PLAIN GS-200208907265200201 —On the market
ENDOTRACHEAL TUBE-PLAIN GS-200208907265200218 —On the market
ENDOTRACHEAL TUBE-PLAIN GS-200208902120200273 —On the market
ENDOTRACHEAL TUBE-RE-INFORCED-CUFFED GS-201308902120201393 —On the market
ENDOTRACHEAL TUBE-RE-INFORCED-CUFFED GS-201308902120201409 —On the market