Taiwan FDA registration 65d919be3a14d363361d94707812cfe0

“HONHI” Impression tube (Non-Sterile)

TW: “鴻海”印模管(未滅菌)

Taiwan·Risk Class 1·MD·KUNSHAN DUAL ADHESIVE PACKAGE INTERNATIONAL TRADE CO., LTD·Registered Oct 01, 2021 – Oct 31, 2024Expired

Registration details

Analysis ID: 65d919be3a14d363361d94707812cfe0
License Form: Ministry of Health Medical Device Land Transport Registration No. 003772
Customs Code: DHA08600377209

Company information

Manufacturer: KUNSHAN DUAL ADHESIVE PACKAGE INTERNATIONAL TRADE CO., LTD
Manufacturer Country: China
Authorized Representative: HONHI MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Impression Tube (F.6570)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F6570 impression tube
Import Information: Imported from abroad; Made in China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2024

About this record

Access comprehensive regulatory information for “HONHI” Impression tube (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 65d919be3a14d363361d94707812cfe0 and manufactured by KUNSHAN DUAL ADHESIVE PACKAGE INTERNATIONAL TRADE CO., LTD. The authorized representative in Taiwan is HONHI MEDICAL CO., LTD..

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