Taiwan FDA registration 49b74e979e65dc0817a068fa99cebe7f

"Teryleaf" Sendo Denture Adhesive (Non-Sterile)

TW: "中美生醫" 仙同假牙黏著劑 (未滅菌)

Taiwan·Risk Class 1·MD·NIPPON ZETTOC CO., LTD.·Registered Jun 01, 2016 – Jun 01, 2021Cancelled

Registration details

Analysis ID: 49b74e979e65dc0817a068fa99cebe7f
License Form: Ministry of Health Medical Device Import No. 016603
Customs Code: DHA09401660300

Company information

Manufacturer: NIPPON ZETTOC CO., LTD.
Manufacturer Country: Japan
Authorized Representative: CHUNG MEI BIOPHARMA CO., LTD.

Product details

Product Type (Level 1): F Dental devices
Product Type (Level 2): F3490 Sodium aminomethylcellulose, and/or polyethylene methyl ether sodium calcium, maleic acid compound salt denture adhesive
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 01, 2016
Expiry Date: Jun 01, 2021
Cancellation Date: Jun 15, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Teryleaf" Sendo Denture Adhesive (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 49b74e979e65dc0817a068fa99cebe7f and manufactured by NIPPON ZETTOC CO., LTD.. The authorized representative in Taiwan is CHUNG MEI BIOPHARMA CO., LTD..

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