Taiwan FDA registration e2ce5c0ee9ed95d54da9359e2205c47b

"Kasamin" uterus probe (sterilization)

TW: "笠民"子宮探條 (滅菌)

Taiwan·Risk Class 1·PANPAC MEDICAL CORPORATION·Registered Aug 01, 2019 – Aug 01, 2024Expired

Registration details

Analysis ID: e2ce5c0ee9ed95d54da9359e2205c47b

Company information

Manufacturer: PANPAC MEDICAL CORPORATION
Manufacturer Country: Taiwan, Province of China
Authorized Representative: RI-MING ENTERPRISES CO., LTD.

Product details

Intended Use: Limited to the classification and grading management of medical equipment "manual instruments for obstetrics and gynecology (L.4530)" the first level identification range.
Product Type (Level 1): l Obstetrics and Gynecology
Product Type (Level 2): L.4530 婦產科專用手動器械
Import Information: 國產;; QMS/QSD;; 委託製造

Dates and status

Registration Date: Aug 01, 2019
Expiry Date: Aug 01, 2024
Cancellation Date: Apr 15, 2024

About this record

Access comprehensive regulatory information for "Kasamin" uterus probe (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e2ce5c0ee9ed95d54da9359e2205c47b and manufactured by PANPAC MEDICAL CORPORATION. The authorized representative in Taiwan is RI-MING ENTERPRISES CO., LTD..

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