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King Vision Video Laryngoscope Standard Blade

FDA UDI

Class I (US FDA UDI)

by King Systems Corporation.

Identity

Trade Name
King Vision Video Laryngoscope Standard Blade FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
Standard disposable blade, size 3 (without channel) Min. purchase 10 pcs. = 1 case FDA UDI
Model / Reference
KVL03 FDA UDI
Description
Standard disposable blade, size 3 (without channel) Min. purchase 10 pcs. = 1 case FDA UDI

Identifiers

Catalog Number
KVL03 FDA UDI
Primary DI / UDI-DI
00612649182131 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

No

FDA UDI

Category: Rigid optical laryngopharyngoscope

King Vision Video Laryngoscope Standard Blade 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 0b6286b0-ab27-4b71-b414-1f33c7f3eb10 36 fields · synced May 30, 2026