Taiwan FDA registration 1951fb5387cc0aefb07aa6c12e5eb255

"Di Cheng" oxygen mask (unsterilized)

TW: "狄成" 氧氣面罩 (未滅菌)

Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Dec 18, 2013 – Dec 18, 2018Cancelled

Registration details

Analysis ID: 1951fb5387cc0aefb07aa6c12e5eb255

Company information

Manufacturer: DI CHENG RUBBER INDUSTRIES INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DI CHENG RUBBER INDUSTRIES INC.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Oxygen Mask (D.5580)".
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5580 Oxygen masks
Import Information: Domestic

Dates and status

Registration Date: Dec 18, 2013
Expiry Date: Dec 18, 2018
Cancellation Date: Aug 05, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Di Cheng" oxygen mask (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1951fb5387cc0aefb07aa6c12e5eb255 and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..

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