"Eagle Labs" Manual Ophthalmic Surgical Instrument (Non-Sterile)
Taiwan·Risk Class 1·MD·EAGLE LABS·Registered Jun 19, 2019 – Jun 19, 2024Expired- Analysis ID
- 4358105a97c51dbc27f5ef0b991cfdff
- License Form
- Ministry of Health Medical Device Import No. 020570
- Customs Code
- DHA09402057000
- Manufacturer
- EAGLE LABS
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT CO., LTD.
- 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
- Registration Date
- Jun 19, 2019
- Expiry Date
- Jun 19, 2024
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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 4358105a97c51dbc27f5ef0b991cfdff and manufactured by EAGLE LABS. The authorized representative in Taiwan is BIOMEGA INSTRUMENT 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.