← Back to catalogue
Tabletop Refraction System TS-310
EUDAMEDFDA UDIClass I (EU MDR)
Ref SS001-0040Model RT-6100,RT-3100,TS-310
Identity
- Trade Name
- Tabletop Refraction System TS-310 EUDAMEDTabletop Refraction System FDA UDI
- Generic Name
- Vision testing/training chart FDA UDI
- Device Name
- The TS-310 is a space-saving automated refraction system that uses a combination of the refractor head of the RT-3100 and a control box. • With the high precision LCD, visual acuity of 5 m as well as near visual acuity of 40 cm can be measured with the same accuracy as a standard refraction using actual distances. • The objective data measured by a NIDEK auto refractometer and the lensometry data measured by a NIDEK lensmeter can be imported and used in this device. FDA UDI
- Model / Reference
- RT-6100,RT-3100,TS-310 EUDAMEDSS001-0040 EUDAMEDTS-310 FDA UDI
- Description
- The TS-310 is a space-saving automated refraction system that uses a combination of the refractor head of the RT-3100 and a control box. • With the high precision LCD, visual acuity of 5 m as well as near visual acuity of 40 cm can be measured with the same accuracy as a standard refraction using actual distances. • The objective data measured by a NIDEK auto refractometer and the lensometry data measured by a NIDEK lensmeter can be imported and used in this device. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987669101414 EUDAMEDFDA UDI
- Basic UDI-DI
- 4987669104G3 EUDAMED
- FDA Product Code
- HKN FDA UDIHOX FDA UDI
- EMDN Code
- Q0299,Z12120115 EUDAMED
- GMDN Term
- Vision testing/training chart FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 886.1770 FDA UDI886.1150 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Tabletop Refraction System TS-310 by Nidek Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4987669104G3 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- NIDEK.CO.Ltd.,
- EUDAMED SRN
- JP-MF-000040151
- Authorised Representative
- NIDEK SA FR-AR-000000341
Sources (2)
- EUDAMED c7303f99-0b36-4776-bdf3-d5e027b80611 61 fields · synced Jul 11, 2026
- FDA UDI 72070dac-f207-4ffa-9003-4a08042692a5 34 fields · synced May 30, 2026