Identity
- Trade Name
- Aurora Surgical Light Series FDA UDI
- Generic Name
- Transportable medical equipment stand, non-powered FDA UDI
- Device Name
- LED Surgical Light with center focus with optional camera capability FDA UDI
- Model / Reference
- Aurora 3 FDA UDI
- Description
- LED Surgical Light with center focus with optional camera capability FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10841736100032 FDA UDI
- FDA Product Code
- FSY FDA UDIFSS FDA UDI
- GMDN Term
- Transportable medical equipment stand, non-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4580 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Aurora Surgical Light Series by Skytron, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Skytron, LLC
Sources (1)
- FDA UDI 173ac4ea-986b-462c-8511-03016ca7eb9a 36 fields · synced May 30, 2026