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King Vision Video Laryngoscope Reusable Display

FDA UDI

Class I (US FDA UDI)

by King Systems Corporation.

Identity

Trade Name
King Vision Video Laryngoscope Reusable Display FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
Reusable, digital display, complete with video-out port and battery status LED indicator FDA UDI
Model / Reference
KVIS01 FDA UDI
Description
Reusable, digital display, complete with video-out port and battery status LED indicator FDA UDI

Identifiers

Catalog Number
KVIS01 FDA UDI
Primary DI / UDI-DI
00612649178059 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid optical laryngopharyngoscope

King Vision Video Laryngoscope Reusable Display by King Systems Corporation. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical laryngopharyngoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
King Systems Corporation.

Sources (1)

  • FDA UDI 1584ca73-2973-495e-b3d1-284401975e19 35 fields · synced May 30, 2026