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Sunkingdom Retinometer

FDA UDI

Class I (US FDA UDI)

by Chongqing Sunkingdom Medical Instrument Co., Ltd

Identity

Trade Name
Sunkingdom Retinometer FDA UDI
Generic Name
Vision testing/training chart FDA UDI
Device Name
Retinometer is mainly used for routine visual function examination (e.g., preoperative visual acuity prediction and postoperative visual acuity recovery assessment for cataracts, glaucoma, retinopathy etc.) FDA UDI
Model / Reference
SK-6500B FDA UDI
Description
Retinometer is mainly used for routine visual function examination (e.g., preoperative visual acuity prediction and postoperative visual acuity recovery assessment for cataracts, glaucoma, retinopathy etc.) FDA UDI

Identifiers

Primary DI / UDI-DI
06973211070923 FDA UDI
FDA Product Code
HOX FDA UDI
GMDN Term
Vision testing/training chart FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1150 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: Vision testing/training chart

Sunkingdom Retinometer by Chongqing Sunkingdom Medical Instrument Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vision testing/training chart.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cbcd621d-b69e-4f81-ac90-cfd60e5d3334 33 fields · synced Jun 8, 2026