← Back to catalogue

King Vision Video Laryngoscope Channeled Blade

FDA UDI

Class I (US FDA UDI)

by King Systems Corporation.

Identity

Trade Name
King Vision Video Laryngoscope Channeled Blade FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
channelled, disposable standard , size 3 Accepts endotracheal tubes from 6.0mm-8.0mm Min. purchase 10 pcs. = 1 case FDA UDI
Model / Reference
KVL03C FDA UDI
Description
channelled, disposable standard , size 3 Accepts endotracheal tubes from 6.0mm-8.0mm Min. purchase 10 pcs. = 1 case FDA UDI

Identifiers

Catalog Number
KVL03C FDA UDI
Primary DI / UDI-DI
00612649182148 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 Channeled 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5562865f-3d42-4978-a843-09c519637df4 36 fields · synced Jun 6, 2026