Identity
- Trade Name
- SightSaverMini FDA UDI
- Generic Name
- Visual stimulator FDA UDI
- Model / Reference
- ATMV001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860003291009 FDA UDI
- 510(k) Number
- K113785 FDA UDI
- FDA Product Code
- GWE FDA UDI
- GMDN Term
- Visual stimulator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1890 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Visual stimulator
SightSaverMini by Anschel Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- USB FLASH ADAPTER CABLE L=5m — EB NEURO SPA · Class II
- Visual System Power Supply — Nordicneurolab · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Anschel Technology, Inc.
Sources (1)
- FDA UDI 862d8be0-d4ce-4795-8527-49aad8d87796 33 fields · synced May 30, 2026