Taiwan FDA registration a99ca1ae04a40a9e694a99ffc0b6c2af

"Membrane Ann" intraoral gel (unsterilized)

TW: “膜安”口內凝膠 (未滅菌)

Taiwan·Risk Class 1·NANOSIGMA BIOTECH. CO., LTD.·Registered Dec 10, 2013 – Dec 10, 2028Active

Registration details

Analysis ID: a99ca1ae04a40a9e694a99ffc0b6c2af

Company information

Manufacturer: NANOSIGMA BIOTECH. CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: VISION RENU CORPORATION

Product details

Intended Use: Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5090 Liquid bandages
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Dec 10, 2013
Expiry Date: Dec 10, 2028

About this record

Access comprehensive regulatory information for "Membrane Ann" intraoral gel (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a99ca1ae04a40a9e694a99ffc0b6c2af and manufactured by NANOSIGMA BIOTECH. CO., LTD.. The authorized representative in Taiwan is VISION RENU CORPORATION.

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