Taiwan FDA registration 1c637f11bfb5534db976a73f2da9657b

"Yongkang" waste liquid collection system (unsterilized)

TW: “永康”廢液收集系統(未滅菌)

Taiwan·Risk Class 1·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Jun 11, 2008 – Jun 11, 2028Active

Registration details

Analysis ID: 1c637f11bfb5534db976a73f2da9657b

Company information

Manufacturer: YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4680 Non-motive, single patient-use, carry-on suctioning device
Import Information: Domestic

Dates and status

Registration Date: Jun 11, 2008
Expiry Date: Jun 11, 2028

About this record

Access comprehensive regulatory information for "Yongkang" waste liquid collection system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c637f11bfb5534db976a73f2da9657b and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..

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