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KC Airway Taping System

FDA UDI

Class I (US FDA UDI)

by KelCor, LLC

Identity

Trade Name
KC Airway Taping System FDA UDI
Generic Name
Multi-purpose surgical skin adhesive tape FDA UDI
Device Name
Short-term Adult Airway Tape and Eye Tape FDA UDI
Model / Reference
KTST-103001 FDA UDI
Description
Short-term Adult Airway Tape and Eye Tape FDA UDI

Identifiers

Primary DI / UDI-DI
00860009651609 FDA UDI
FDA Product Code
CBH FDA UDI
HOY FDA UDI
GMDN Term
Multi-purpose surgical skin adhesive tape FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 FDA UDI
886.4750 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose surgical skin adhesive tapeEye patch

KC Airway Taping System by KelCor, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye patch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KelCor, LLC

Sources (1)

  • FDA UDI 65763f08-cc20-499e-b423-336aa6e75a9b 35 fields · synced May 29, 2026