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VisiChart

FDA UDI

Class I (US FDA UDI)

by Topcon Healthcare, Inc.

Identity

Trade Name
VisiChart FDA UDI
Generic Name
Visual acuity projector FDA UDI
Device Name
Visual Acuity Chart FDA UDI
Model / Reference
VisiChart II FDA UDI
Description
Visual Acuity Chart FDA UDI

Identifiers

Primary DI / UDI-DI
00850053428500 FDA UDI
FDA Product Code
HOS FDA UDI
GMDN Term
Visual acuity projector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Visual acuity projector

VisiChart by Topcon Healthcare, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Visual acuity projector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d993006-44e5-4cac-b08d-e468671d4416 33 fields · synced May 29, 2026