Taiwan FDA registration dc4d1f4b1503a34bb6f18bd6a9fe7dfe
"Medeli" RF host and accessories
TW: “美德力”射頻主機及配件
Registration details
- Analysis ID
- dc4d1f4b1503a34bb6f18bd6a9fe7dfe
- Customs Code
- DHA05602974100
Company information
- Manufacturer
- Mederi RF LLC;; Sanmina Corporation
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- This product is used with the Stretta Catheter catheter for the treatment of gastroesophageal reflux disorders.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- May 05, 2017
- Expiry Date
- May 05, 2027
About this record
Access comprehensive regulatory information for "Medeli" RF host and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc4d1f4b1503a34bb6f18bd6a9fe7dfe and manufactured by Mederi RF LLC;; Sanmina Corporation. The authorized representative in Taiwan is Huizhong 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