The 3-stage timeframe for UDI system implementation was initiated on June 1st, 2021. Class 3 implantable medical devices are the first batch of products to adapt UDI. Afterward, Class 3 non-implantable medical devices have to integrate with the UDI system beginning on June 1st, 2022. Finally, until earlier this year, Class 2 medical devices shall comply with all UDI regulations and requirements starting from June 1st, 2023. 


Holders of medical device licenses should upload the Device Identifier (DI) and other related medical device information onto the Taiwan UDID platform before importing or distributing the products.

Timeframe of UDI System Implementation:

Stage

Enforcement Date

Medical Devices

Stage 1

June 1st, 2021

Class 3 implantable medical devices

Stage 2

June 1st, 2022

Class 3 non-implantable medical devices

Stage 3

June 1st, 2023

Class 2 medical devices

The following kinds of medical devices are not required to integrate UDI:

1.

Customized medical devices.

2.

Medical devices specifically for export only.

3.

Single-use and non-standalone or non-implantable medical device components that are sold with a medical device combination kit or in vitro diagnostic medical device.

The following medical device classifications are not required to label PI (Production Identifier):

Item

Classification No.

Classification Name

1

E.1120

Blood pressure cuff

2

E.2770

Medical Impedance plethysmograph

3

G.5220

Ear, nose, and throat drug administration device

4

I.0004

Alcohol pad

5

I.0005

Providone-Iodine pad

6

I.4014

Nonresorbable gauze/sponge for external use

7

I.4040

Medical apparel

8

J.0001

Saline solution for wound irrigation

9

J.2910

Clinical electronic thermometer

10

J.5240

Medical adhesive tape and adhesive bandage

11

J.5780

Medical support stocking

12

L.5300

Condom

13

L.5310

Condom with spermicidal lubricant

14

L.5400

Menstrual cup

15

L.5460

Scented or scented deodorized menstrual tampon

16

L.5470

Unscented menstrual tampon

17

M.5925

Soft (hydrophilic) contact lens

18

M.5916

Rigid gas permeable contact lens

19

M.5918

Rigid gas permeable contact lens care products

20

M.5928

Soft (hydrophilic) contact lens care products

21

O.3800

Motorized vehicle for medical purposes

22

O.3860

Powered wheelchair

 

 

Reference:

TFDA Announcement: Implementation of “Requirements for Indicating the Unique Device Identifier on Medical Device Labels”

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