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Oc-2300

FDA UDI

Class I (US FDA UDI)

by Topcon Healthcare, Inc.

Identity

Trade Name
OC-2300 FDA UDI
Generic Name
Ophthalmic chair, line-powered FDA UDI
Device Name
OC-2300 CHAIR BLACK 120V LOW WIRELESS; Ophthalmic examination chair FDA UDI
Model / Reference
24045-BL-L1-011 FDA UDI
Description
OC-2300 CHAIR BLACK 120V LOW WIRELESS; Ophthalmic examination chair FDA UDI

Identifiers

Primary DI / UDI-DI
00850053428562 FDA UDI
FDA Product Code
HME FDA UDI
GMDN Term
Ophthalmic chair, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1140 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: Ophthalmic chair, line-powered

Oc-2300 by Topcon Healthcare, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic chair, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c6ab6773-7181-4aea-9ef0-5820184bcdff 33 fields · synced Jun 1, 2026