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Procedure Pack, product family

by GRI Medical & Electronic Technology Co., Ltd. 6 variants Basic UDI-DI 69319181F080L9

Shared by every variant

Basic UDI-DI
69319181F080L9
Risk class
Class I
Legislation
MDR
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 69319181F080L9.

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 Procedure Pack, Basic UDI-DI 69319181F080L9
UDI-DISize and differences
Procedure Pack 86-01527-S / ORT-0116931918155173 —On the market
Procedure Pack 86-09206-S / ORT-0116931918161822 —On the market
Procedure Pack 86-09208-S / ORT-0116931918134482 —On the market
Procedure Pack 86-09209-S / ORT-0116931918199849 —On the market
Procedure Pack 86-09308-S / ORT-0116931918178424 —On the market
Procedure Pack 86-09514-S / ORT-0116931918198804 —On the market