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NAKANISHI INC. devices, product family

by NAKANISHI INC. 11 variants Basic UDI-DI 456022499000000074

Shared by every variant

Manufacturer
NAKANISHI INC.(11)
Basic UDI-DI
456022499000000074
Risk class
Class IIa
Legislation
MDR
EMDN category
INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIESQ0199,Z12110102,Z12110180
Market status
8 on the market3 not intended for the eu market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 456022499000000074.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 11 devices listed on this page; other pages of the family can carry others.

Variants

11 devices · page 1 of 1

Variants of NAKANISHI INC. devices, Basic UDI-DI 456022499000000074
UDI-DISize and differences
Y1004195 Y1004195 / SPP000000004589551393404
Sterilised before use: yes
On the market
Y1004196 Y1004196 / SPP000000004589551393411
Sterilised before use: yes
On the market
Y1500399 Y1500399 / SPP000000004589551392483
Sterilised before use: yes
Not intended for the EU market
Y1500511 Y1500511 / SPP000000004589551396375
Sterilised before use: yes
Not intended for the EU market
Y1500512 Y1500512 / SPP000000004589551396382
Sterilised before use: yes
Not intended for the EU market
Y1500515 Y1500515 / SPP000000004589551396177
Sterilised before use: yes
On the market
Y1500516 Y1500516 / SPP000000004589551396184
Sterilised before use: yes
On the market
Y1500766 Y1500766 / SPP000000004589551389742
Sterilised before use: yes
On the market
Y1500803 Y1500803 / SPP000000004589551390311
Sterilised before use: yes
On the market
Y1500872G Y1500872G / SPP000000004589551392650
Sterilised before use: yes
On the market
Y1501018 Y1501018 / SPP000000004589551393527
Sterilised before use: no
On the market