Taiwan FDA registration 15737c505b396eb57f09fa3d27bfc7c9

"K.F." Splint(Non-Sterile)

TW: "國發"固定帶(未滅菌)

Taiwan·Risk Class 1·MD·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: 15737c505b396eb57f09fa3d27bfc7c9
License Form: Ministry of Health Medical Device Manufacturing Registration No. 000482
Customs Code: DHY08300048204

Company information

Manufacturer: K.F. MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: K.F. MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: It is used to support or immobilize fractures, injuries with excessive force or sprains to the trunk.
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3490 Torso Gear
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for "K.F." Splint(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 15737c505b396eb57f09fa3d27bfc7c9 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS CO., LTD..

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