Taiwan FDA registration 9b1f0b6c4b6754cf064edaec4980286b

"Zhuli" manual instrument for general surgery (not sterilized)

TW: "朵莉" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·TULIP MEDICAL PRODUCTS·Registered Jan 30, 2016 – Jan 30, 2026Expired

Registration details

Analysis ID: 9b1f0b6c4b6754cf064edaec4980286b
Customs Code: DHA09401613302

Company information

Manufacturer: TULIP MEDICAL PRODUCTS
Manufacturer Country: United States
Authorized Representative: RUBY-JANE INTERNATIONAL CORPORATION

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Jan 30, 2016
Expiry Date: Jan 30, 2026
Cancellation Date: Nov 14, 2024

About this record

Access comprehensive regulatory information for "Zhuli" manual instrument for general surgery (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b1f0b6c4b6754cf064edaec4980286b and manufactured by TULIP MEDICAL PRODUCTS. The authorized representative in Taiwan is RUBY-JANE INTERNATIONAL CORPORATION.

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