Taiwan FDA registration b56a4a854af2029b76bb929183d8e0d9

"Eagle Labs" Manual Ophthalmic Surgical Instrument (Non-Sterile)

TW: "伊勾雷博斯" 手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·EAGLE LABS·Registered Aug 22, 2018 – Aug 22, 2023Expired
Registration details
Analysis ID
b56a4a854af2029b76bb929183d8e0d9
License Form
Ministry of Health Medical Device Import No. 019528
Customs Code
DHA09401952801
Company information
Manufacturer
EAGLE LABS
Manufacturer Country
United States
Authorized Representative
ZhiKeco Co., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4350 Manual Ophthalmic Surgery Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 22, 2018
Expiry Date
Aug 22, 2023
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About this record

Access comprehensive regulatory information for "Eagle Labs" Manual Ophthalmic Surgical Instrument (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 b56a4a854af2029b76bb929183d8e0d9 and manufactured by EAGLE LABS. The authorized representative in Taiwan is ZhiKeco Co., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EAGLE LABS, 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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