Taiwan FDA registration 0d66d6cc51042531f551da0f20d1abac
Daejeon plastic portable stretcher (unsterilized)
TW: 大田牌塑膠手提式擔架(未滅菌)
Taiwan·Risk Class 1·AMERICA BUSINESS OF CALIFONIA·Registered Oct 30, 2005 – Oct 30, 2020CancelledRegistration details
- Analysis ID
- 0d66d6cc51042531f551da0f20d1abac
- Customs Code
- DHA04400157306
Company information
- Manufacturer
- AMERICA BUSINESS OF CALIFONIA
- Manufacturer Country
- United States
- Authorized Representative
- EZ-CARE INSTRUMENTS. CO., LTD.
Product details
- Intended Use
- The portable stretcher is made of high-density polyethylene integrally molded, which is suitable for carrying patients with accidental injuries, injuries or fainting.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6900 Hand-held stretcher
- Import Information
- import
Dates and status
- Registration Date
- Oct 30, 2005
- Expiry Date
- Oct 30, 2020
- 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 Daejeon plastic portable stretcher (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d66d6cc51042531f551da0f20d1abac and manufactured by AMERICA BUSINESS OF CALIFONIA. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices