Taiwan FDA registration ce83573053a6be0d5e8c28abbefa8668
“Rusch” Bronchus Blocker Set
TW: “路希”支氣管內管阻隔器組
Taiwan·Risk Class 2·MD·WILLY RUSCH GMBH·Registered Dec 24, 2015 – Dec 24, 2020CancelledRegistration details
- Analysis ID
- ce83573053a6be0d5e8c28abbefa8668
- License Form
- Ministry of Health Medical Device Import No. 028120
- Customs Code
- DHA05602812002
Company information
- Manufacturer
- WILLY RUSCH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5740 Trachea/bronchial divergence ventilation line
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 24, 2015
- Expiry Date
- Dec 24, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Rusch” Bronchus Blocker Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce83573053a6be0d5e8c28abbefa8668 and manufactured by WILLY RUSCH GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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