Identity
- Trade Name
- OCULUS Easyfield VR FDA UDI
- Generic Name
- Visual acuity projector FDA UDI
- Model / Reference
- OCVR-01 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850040295818 FDA UDI
- FDA Product Code
- QTO FDA UDI
- GMDN Term
- Visual acuity projector FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1150 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Visual acuity projector
OCULUS Easyfield VR by The Hilsinger Company Parent, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- YEASN — Chongqing Yeasn Science & Technology Co., Ltd. · 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
- The Hilsinger Company Parent, LLC
Sources (1)
- FDA UDI e7c2d914-b265-4a5f-a9d0-9bc86ec4b627 33 fields · synced May 30, 2026