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King Vision Video Laryngoscope Standard aBlade

FDA UDI

Class I (US FDA UDI)

by King Systems Corporation.

Identity

Trade Name
King Vision Video Laryngoscope Standard aBlade FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
King Vision - aBlades size 3 20 pcs. = 1 case FDA UDI
Model / Reference
KVLAB3 FDA UDI
Description
King Vision - aBlades size 3 20 pcs. = 1 case FDA UDI

Identifiers

Catalog Number
KVLAB3 FDA UDI
Primary DI / UDI-DI
00612649181226 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rigid optical laryngopharyngoscope

King Vision Video Laryngoscope Standard aBlade 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 54189e37-5991-4da0-8a6e-21f3b8a179a1 36 fields · synced May 30, 2026