Identity
- Trade Name
- KC Eye Tape FDA UDI
- Generic Name
- Eye patch FDA UDI
- Device Name
- Adult Eye Tape FDA UDI
- Model / Reference
- EYST-300020 FDA UDI
- Description
- Adult Eye Tape FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860009651616 FDA UDI
- FDA Product Code
- HOY FDA UDI
- GMDN Term
- Eye patch FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye patch
KC Eye Tape by KelCor, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Eye patch.
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- Sharn Inc — Sharn Anesthesia · Class I
- iPRO — FANNIN (UK) LIMITED · Class I
- Optego — Optego Vision USA, Inc. · Class I
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 8d30f5c1-34af-42b6-8da5-1902d0cbece4 35 fields · synced May 30, 2026