Taiwan FDA registration c580122d4ddf81e18c61405e267ba57b

"GULDEN" Ophthalmic bar prism (Non-Sterile)

TW: "古登" 眼科用棒狀稜鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·GULDEN OPHTHALMICS·Registered Nov 16, 2020 – Nov 16, 2025Expired
Registration details
Analysis ID
c580122d4ddf81e18c61405e267ba57b
License Form
Ministry of Health Medical Device Import No. 022112
Customs Code
DHA09402211206
Company information
Manufacturer
GULDEN OPHTHALMICS
Manufacturer Country
United States
Authorized Representative
HATCHELL CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of rod prism (M.1650) for ophthalmology under the management measures for medical equipment.
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1650 Rod prism for ophthalmology
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 16, 2020
Expiry Date
Nov 16, 2025
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About this record

Access comprehensive regulatory information for "GULDEN" Ophthalmic bar prism (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c580122d4ddf81e18c61405e267ba57b and manufactured by GULDEN OPHTHALMICS. The authorized representative in Taiwan is HATCHELL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GULDEN OPHTHALMICS, and 1 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.

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