Taiwan FDA registration 2ef7d37efda4a9ef22d9a91591624b8a
“ASAHI” Peripheral Guide Wire
TW: “朝日”周邊血管導引線
Taiwan·Risk Class 2·MD·ASAHI INTECC(THAILAND) CO., LTD·Registered Dec 28, 2017 – Dec 28, 2027ActiveRegistration details
- Analysis ID
- 2ef7d37efda4a9ef22d9a91591624b8a
- License Form
- Ministry of Health Medical Device Import No. 030634
- Customs Code
- DHA05603063402
Company information
- Manufacturer
- ASAHI INTECC(THAILAND) CO., LTD
- Manufacturer Country
- Thailand
- Authorized Representative
- ASAHI INTECC CO.,LTD. TAIWAN BRANCH (JAPAN)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 28, 2017
- Expiry Date
- Dec 28, 2027
About this record
Access comprehensive regulatory information for “ASAHI” Peripheral Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2ef7d37efda4a9ef22d9a91591624b8a and manufactured by ASAHI INTECC(THAILAND) CO., LTD. The authorized representative in Taiwan is ASAHI INTECC CO.,LTD. TAIWAN BRANCH (JAPAN).
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