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Visionix

FDA UDI

Class II (US FDA UDI)

by Right Mfg. Co., Ltd.

Identity

Trade Name
Visionix FDA UDI
Generic Name
Ophthalmic examination slit lamp FDA UDI
Device Name
CLINICAL UNIT SET FDA UDI
Model / Reference
MW50D FDA UDI
Description
CLINICAL UNIT SET FDA UDI

Identifiers

Catalog Number
VSN5800NB FDA UDI
Primary DI / UDI-DI
04580606431522 FDA UDI
510(k) Number
K110129 FDA UDI
FDA Product Code
HJO FDA UDI
GMDN Term
Ophthalmic examination slit lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1850 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 350 Millimeter FDA UDI
Depth — 387 Millimeter FDA UDI
Height — 678.5 Millimeter FDA UDI
Weight — 14 Kilogram FDA UDI

Category: Ophthalmic examination slit lamp

Visionix by Right Mfg. Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic examination slit lamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5b36113e-2075-485a-a2d4-efd7eab16953 37 fields · synced May 30, 2026