Identity
- Trade Name
- PalmScan VF2000 FDA UDI
- Generic Name
- Perimeter, automatic FDA UDI
- Device Name
- Virtual reality based battery powered automatically operated, diagnostic, ophthalmic instrument intended for assessing the extent of the patient's peripheral visual field. Small luminous points (spots) are automatically displayed in various random positions and patient response is automatically recorded. The print-out (chart) then shows the resulting curve of the visual field. FDA UDI
- Model / Reference
- VF2000 FDA UDI
- Description
- Virtual reality based battery powered automatically operated, diagnostic, ophthalmic instrument intended for assessing the extent of the patient's peripheral visual field. Small luminous points (spots) are automatically displayed in various random positions and patient response is automatically recorded. The print-out (chart) then shows the resulting curve of the visual field. FDA UDI
Identifiers
- Catalog Number
- 900-0015-01 FDA UDI
- Primary DI / UDI-DI
- 00853569007108 FDA UDI
- FDA Product Code
- HPT FDA UDI
- GMDN Term
- Perimeter, automatic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1605 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
Yes
FDA UDI
Category: Perimeter, automatic
PalmScan VF2000 by Micro Medical Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Perimeter, automatic.
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- COMPASS — CENTERVUE S.P.A. · Class IIa
- Virtual Eye Software — VIRTUAL VISION HEALTH · Class I
- Virtual Field — Field Virtual Inc · Class I
- VisionOne — PeriVision SA · Class I
- Twinfield 3 — OCULUS Optikgeräte GmbH · Class I
- Humphrey Field Analyzer 3 (HFA3) — Carl Zeiss Meditec AG · 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
- Micro Medical Devices, Inc.
Sources (1)
- FDA UDI 200ddf1f-e5f0-433d-a881-900674d528c3 36 fields · synced Jun 8, 2026