Taiwan FDA registration 92397856bb0667f4765a6b31d09894d3

"Rumex" Manual ophthalmic surgical instrument (Sterile)

TW: "羅美思" 手動式眼科手術器械 (滅菌)

Taiwan·Risk Class 1·MD·RUMEX INTERNATIONAL LTD·Registered Aug 13, 2019 – Aug 13, 2024Expired

Registration details

Analysis ID: 92397856bb0667f4765a6b31d09894d3
License Form: Ministry of Health Medical Device Import No. 020746
Customs Code: DHA09402074601

Company information

Manufacturer: RUMEX INTERNATIONAL LTD
Manufacturer Country: United Kingdom
Authorized Representative: BIOMEGA INSTRUMENT 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 13, 2019
Expiry Date: Aug 13, 2024

About this record

Access comprehensive regulatory information for "Rumex" Manual ophthalmic surgical instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 92397856bb0667f4765a6b31d09894d3 and manufactured by RUMEX INTERNATIONAL LTD. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

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