← Back to catalogue

Video laryngoscope reusable display and adapter

FDA UDI

Class I (US FDA UDI)

by King Systems Corporation.

Identity

Trade Name
Video laryngoscope reusable display and adapter FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
Display and Adapter Kit - for King Vision Includes 1 Display and 1 Adapter 3-4 FDA UDI
Model / Reference
KVIS01VA34 FDA UDI
Description
Display and Adapter Kit - for King Vision Includes 1 Display and 1 Adapter 3-4 FDA UDI

Identifiers

Catalog Number
KVIS01VA34 FDA UDI
Primary DI / UDI-DI
00612649181257 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

Yes

FDA UDI

Category: Rigid optical laryngopharyngoscope

Video laryngoscope reusable display and adapter 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

Manufacturer
King Systems Corporation.

Sources (1)

  • FDA UDI 63ff7ff4-8d10-49ef-9414-036735548def 36 fields · synced Jun 1, 2026