Identity
- Trade Name
- IBEX Keratometer FDA UDI
- Generic Name
- Keratoscope, powered FDA UDI
- Device Name
- IBEX Keratometer is used for measuring the curvature of the anterior surface of the cornea, particularly for assessing the extent and axis of astigmatism. FDA UDI
- Model / Reference
- MK FDA UDI
- Description
- IBEX Keratometer is used for measuring the curvature of the anterior surface of the cornea, particularly for assessing the extent and axis of astigmatism. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00869228000472 FDA UDI
- FDA Product Code
- HLQ FDA UDI
- GMDN Term
- Keratoscope, powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1350 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Keratoscope, powered
IBEX Keratometer by Trevi Technology — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Keratoscope, powered.
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
- Trevi Technology
Sources (1)
- FDA UDI 044a31e8-d075-44f1-a31e-a1a22ac72451 34 fields · synced Jun 8, 2026