Taiwan FDA registration 6a051924df50f2eb918f0d64da123ce1

"默罕" manual instrument for general surgery (sterilization)

TW: "默罕" 一般手術用手動式器械 (滅菌)

Taiwan·Risk Class 1·MOOHAN ENTERPRISE CO., LTD.·Registered Dec 03, 2019 – Dec 03, 2029Active

Registration details

Analysis ID: 6a051924df50f2eb918f0d64da123ce1
Customs Code: DHA09402106505

Company information

Manufacturer: MOOHAN ENTERPRISE CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: MEDI-CORE BIOTECH CO., LTD.

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: Input;; QMS/QSD

Dates and status

Registration Date: Dec 03, 2019
Expiry Date: Dec 03, 2029

About this record

Access comprehensive regulatory information for "默罕" manual instrument for general surgery (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6a051924df50f2eb918f0d64da123ce1 and manufactured by MOOHAN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is MEDI-CORE BIOTECH CO., LTD..

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