Taiwan FDA registration fd6cb024c849eb7864f5363f9b52f7b3

General manual instruments for "Telifes" obstetrics and gynecology (unsterilized)　

TW: “泰利芙斯”婦產科用一般手動器械 (未滅菌)　

Taiwan·Risk Class 1·Teleflex Medical·Registered Apr 08, 2011 – Apr 08, 2026Expired

Registration details

Analysis ID: fd6cb024c849eb7864f5363f9b52f7b3
Customs Code: DHA04401016100

Company information

Manufacturer: Teleflex Medical
Manufacturer Country: United States
Authorized Representative: ASIA EAGLE CO., LTD.

Product details

Intended Use: It is limited to the first-level identification scope of the "General Manual Instruments for Obstetrics and Gynecology (L.4520)" Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): l Obstetrics and Gynecology
Product Type (Level 2): L.4520 婦產科用一般手動器械
Import Information: import

Dates and status

Registration Date: Apr 08, 2011
Expiry Date: Apr 08, 2026

About this record

Access comprehensive regulatory information for General manual instruments for "Telifes" obstetrics and gynecology (unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd6cb024c849eb7864f5363f9b52f7b3 and manufactured by Teleflex Medical. The authorized representative in Taiwan is ASIA EAGLE CO., LTD..

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