Taiwan FDA registration 080caa16282053954ee33230aa5727e9
"Abbott" Anyouwei Leadless Rhythm Delivers/Removes Catheters
TW: “雅培” 安又威無導線節律器遞送/移除導管
Registration details
- Analysis ID
- 080caa16282053954ee33230aa5727e9
- Customs Code
- DHA05603633901
Company information
- Manufacturer
- ABBOTT MEDICAL;; Abbott Medical
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Medical Taiwan Co.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3610 Pulsator of implantable cardiac rhythm apparatus
- Import Information
- import
Dates and status
- Registration Date
- Apr 05, 2023
- Expiry Date
- Apr 05, 2028
About this record
Access comprehensive regulatory information for "Abbott" Anyouwei Leadless Rhythm Delivers/Removes Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 080caa16282053954ee33230aa5727e9 and manufactured by ABBOTT MEDICAL;; Abbott Medical. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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