Taiwan FDA registration 8123450df7175b93cdb8564bee03a972
"East China" diagnostic X-ray tube bulb (unsterilized)
TW: “華東”診斷用X光管球 (未滅菌)
Registration details
- Analysis ID
- 8123450df7175b93cdb8564bee03a972
- Customs Code
- DHAS4600139608
Company information
- Manufacturer Country
- China
- Authorized Representative
- LITE-MED INC.
Product details
- Intended Use
- Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1760 診斷用X光球管套組件
- Import Information
- Chinese goods;; Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Jun 30, 2011
- Expiry Date
- Jun 30, 2026
About this record
Access comprehensive regulatory information for "East China" diagnostic X-ray tube bulb (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8123450df7175b93cdb8564bee03a972 and manufactured by NANJING HUADONG ELECTRONICS GROUP MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is LITE-MED INC..
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