Taiwan FDA registration 6e9c18c4b7ec6c3cc315888199fc30d2
"FERNO" Stretcher (Non-Sterile)
TW: "費諾" 手提式擔架 (未滅菌)
Taiwan·Risk Class 1·MD·FERNO-WASHINGTON, INC.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 6e9c18c4b7ec6c3cc315888199fc30d2
- License Form
- Ministry of Health Medical Device Import Registration No. 010070
- Customs Code
- DHA08401007004
Company information
- Manufacturer
- FERNO-WASHINGTON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ADEPT GENERAL CORP.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- 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" Stretcher (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 6e9c18c4b7ec6c3cc315888199fc30d2 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..
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