"Fujifilm" electronic bronchoscope
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Jun 06, 2012 – Jun 06, 2027Active- Analysis ID
- c2761da94ef24c967f73e64382a26eee
- Customs Code
- DHA00602361001
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
- Import Information
- import
- Registration Date
- Jun 06, 2012
- Expiry Date
- Jun 06, 2027
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Access comprehensive regulatory information for "Fujifilm" electronic bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c2761da94ef24c967f73e64382a26eee and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, and 2 recent registrations in the same category. 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.