Taiwan FDA registration 8a95c9d53c136d40440a78d779cc6d27

OKcare Multi-Frequency Therapy Device

TW: 歐克週波治療器

Taiwan·Risk Class 2·MD·OK BIOTECH CO., LTD.·Registered Mar 02, 2021 – Mar 02, 2026Expired

Registration details

Analysis ID: 8a95c9d53c136d40440a78d779cc6d27
License Form: Ministry of Health Medical Device Manufacturing No. 007077

Company information

Manufacturer: OK BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: OK BIOTECH CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): K Devices for neuroscience
Product Type (Level 2): K5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Mar 02, 2021
Expiry Date: Mar 02, 2026

About this record

Access comprehensive regulatory information for OKcare Multi-Frequency Therapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a95c9d53c136d40440a78d779cc6d27 and manufactured by OK BIOTECH CO., LTD.. The authorized representative in Taiwan is OK BIOTECH CO., LTD..

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