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Auto Refractometer

EUDAMEDFDA UDI

Class I (EU MDR)

Ref RM-800

by Topcon Corporation

Identity

Trade Name
AUTO REFRACTOMETER RM-800 FDA UDI
Generic Name
Automated ophthalmic refractometer FDA UDI
Device Name
AUTO REFRACTOMETER EUDAMED
Model / Reference
RM-800 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04571130283374 EUDAMEDFDA UDI
Basic UDI-DI
4560126260050U6 EUDAMED
FDA Product Code
HKO FDA UDI
EMDN Code
Z12120115 OPTOMETERS EUDAMED
GMDN Term
Automated ophthalmic refractometer FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.1760 FDA UDI
Market of Registration
Netherlands 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

Yes

FDA UDI

Auto Refractometer by Topcon Corporation — 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

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Manufacturer

Manufacturer
Topcon Corporation
EUDAMED SRN
JP-MF-000003928
Authorised Representative
Topcon Europe Medical BV NL-AR-000000441

Sources (2)

  • EUDAMED fe3d1fba-6fa0-4f34-8f49-9d64c868e651 61 fields · synced Jun 18, 2026
  • FDA UDI faf0746d-9814-4e40-ba62-e4db99fd4934 32 fields · synced May 29, 2026