Taiwan FDA registration cc4173784383cff69826076c49d4651c
Guxi disposable sterile antimony moxibustion needle
TW: 古溪一次性無菌鍼灸針
Registration details
- Analysis ID
- cc4173784383cff69826076c49d4651c
- Customs Code
- DHA09200118401
Company information
- Manufacturer
- Maanshan Bond Medical Instruments Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- Glory Medical Equipment & Materials Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5580 Needle moxibustion needle
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Oct 12, 2020
- Expiry Date
- Oct 12, 2025
About this record
Access comprehensive regulatory information for Guxi disposable sterile antimony moxibustion needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc4173784383cff69826076c49d4651c and manufactured by Maanshan Bond Medical Instruments Co., Ltd.. The authorized representative in Taiwan is Glory Medical Equipment & Materials 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.
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