Taiwan FDA registration 20e5cd7f352ca0b5edc5fc6e6bcb80ef
Liftable cardiac shock Su Composer
TW: 可提式心臟電擊蘇復器
Taiwan·QUINTON INSTRUMENT CO.·Registered Jun 15, 1991 – Jun 15, 1996CancelledRegistration details
- Analysis ID
- 20e5cd7f352ca0b5edc5fc6e6bcb80ef
- Customs Code
- DHA00600635004
Company information
- Manufacturer
- QUINTON INSTRUMENT CO.
- Manufacturer Country
- United States
- Authorized Representative
- Pomei Enterprise Co., Ltd
Product details
- Product Type (Level 1)
- 0610 Cardiac shock resuscitation compounder
- Import Information
- import
Dates and status
- Registration Date
- Jun 15, 1991
- Expiry Date
- Jun 15, 1996
- Cancellation Date
- Oct 06, 1999
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者;;改列無須辦理查驗之醫療器材
About this record
Access comprehensive regulatory information for Liftable cardiac shock Su Composer in Taiwan's medical device market through Pure Global AI's free database. is registered under number 20e5cd7f352ca0b5edc5fc6e6bcb80ef and manufactured by QUINTON INSTRUMENT CO.. The authorized representative in Taiwan is Pomei Enterprise 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