Taiwan FDA registration e533781ddf091a4a09876d941ee68ad8
"Nidek" Digital PD Meter(Non-Sterile)
TW: "尼德克"瞳距儀(未滅菌)
Taiwan·Risk Class 1·MD·NIDEK CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- e533781ddf091a4a09876d941ee68ad8
- License Form
- Ministry of Health Medical Device Import Registration No. 010246
- Customs Code
- DHA08401024602
Company information
- Manufacturer
- NIDEK CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the "Pupil Meter (M.1700)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1700 Pupillometer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Nidek" Digital PD Meter(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 e533781ddf091a4a09876d941ee68ad8 and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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