Taiwan FDA registration 3092f4e712cfc21af208caaa11fd3b41
"FERNO" NAJO Backboard(Non-Sterile)
TW: "費諾"長背板(未滅菌)
Taiwan·Risk Class 1·MD·FERNO-WASHINGTON, INC.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 3092f4e712cfc21af208caaa11fd3b41
- License Form
- Ministry of Health Medical Device Import Registration No. 010068
- Customs Code
- DHA08401006804
Company information
- Manufacturer
- FERNO-WASHINGTON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ADEPT GENERAL CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6900 portable stretcher
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "FERNO" NAJO Backboard(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 3092f4e712cfc21af208caaa11fd3b41 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..
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