Taiwan FDA registration f054dbe6680c3718ab92392b205e2bc7

"Bonthe" otolaryngology foam (sterilization)

TW: "邦特" 耳鼻喉科用泡棉 (滅菌)

Taiwan·Risk Class 1·CENEFOM CORP.·Registered Dec 01, 2016 – Dec 01, 2021Cancelled

Registration details

Analysis ID: f054dbe6680c3718ab92392b205e2bc7

Company information

Manufacturer: CENEFOM CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BIOTEQUE CORPORATION

Product details

Intended Use: Limited to the first level of identification scope of "external use of non-absorbent gauze or sponge balls (I.4014)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4014 Non-absorbent cloth or sea balls are used externally
Import Information: 國產;; QMS/QSD;; 委託製造

Dates and status

Registration Date: Dec 01, 2016
Expiry Date: Dec 01, 2021
Cancellation Date: Sep 11, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Bonthe" otolaryngology foam (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f054dbe6680c3718ab92392b205e2bc7 and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is BIOTEQUE CORPORATION.

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