Taiwan FDA registration e55b24cd75f0fd9f8504d9f701e9fb27

"Dayi" non-AC electric patient lift bed (unsterilized)

TW: “大億”非交流電動病患移位床 (未滅菌)

Taiwan·Risk Class 1·Dayi Medical Instrument Factory·Registered Feb 04, 2009 – Feb 04, 2014Cancelled

Registration details

Analysis ID: e55b24cd75f0fd9f8504d9f701e9fb27

Company information

Manufacturer: Dayi Medical Instrument Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Dayi Medical Instrument Factory

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5510 Non-AC electric patient lifts
Import Information: Domestic

Dates and status

Registration Date: Feb 04, 2009
Expiry Date: Feb 04, 2014
Cancellation Date: Dec 14, 2016

Cancellation information

Status: Logged out
Reason: 屆期未申請展延

About this record

Access comprehensive regulatory information for "Dayi" non-AC electric patient lift bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e55b24cd75f0fd9f8504d9f701e9fb27 and manufactured by Dayi Medical Instrument Factory. The authorized representative in Taiwan is Dayi Medical Instrument Factory.

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