← Back to catalogue
Auto Refractometer Ar-F
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 30641-0A40,30641-0B40,30641-0C40,30641-0D40,30641-0E40,30641-0F40Model AR-1,AR-1a,AR-1s,HandyRef,AR-F
Identity
- Trade Name
- AUTO REFRACTOMETER AR-F EUDAMEDAUTO REFRACTOMETER FDA UDI
- Generic Name
- Automated ophthalmic refractometer FDA UDI
- Device Name
- The AUTO REFRACTOMETER AR-F is a medical device which measures objective refractive errors of the patient’s eye. This device also offers retroillumination mode for observing the condition of the ocular media, and measures the amplitude of accommodation. FDA UDI
- Model / Reference
- AR-1,AR-1a,AR-1s,HandyRef,AR-F EUDAMED30641-0A40,30641-0B40,30641-0C40,30641-0D40,30641-0E40,30641-0F40 EUDAMEDAR-F FDA UDI
- Description
- The AUTO REFRACTOMETER AR-F is a medical device which measures objective refractive errors of the patient’s eye. This device also offers retroillumination mode for observing the condition of the ocular media, and measures the amplitude of accommodation. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987669101469 EUDAMEDFDA UDI
- Basic UDI-DI
- 4987669201G2 EUDAMED
- FDA Product Code
- HKO FDA UDI
- EMDN Code
- Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
- GMDN Term
- Automated ophthalmic refractometer FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 886.1760 FDA UDI
- Market of Registration
- France 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
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
Auto Refractometer Ar-F by Nidek Co., Ltd. — Class IIa — 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 | 4987669201G2 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | 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 (3)
- EUDAMED e542e614-0f39-4843-8167-677fb9dd4e03 61 fields · synced Jun 19, 2026
- FDA UDI 7b6312f2-a0a9-4753-bb57-3b77a0a92b3e 34 fields · synced May 30, 2026
- EUDAMED e542e614-0f39-4843-8167-677fb9dd4e03-1 61 fields · synced Jun 10, 2026