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 UDIHOY FDA UDI
- GMDN Term
- Multi-purpose surgical skin adhesive tape FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5770 FDA UDI886.4750 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
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- KelCor, LLC
Sources (1)
- FDA UDI 65763f08-cc20-499e-b423-336aa6e75a9b 35 fields · synced May 29, 2026