Identity
- Trade Name
- AMNOTEC FDA UDI
- Generic Name
- Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
- Device Name
- VEQTRON ICG/NIR 4K Twinlight LED-Laser Light Source FDA UDI
- Model / Reference
- 71-182-30 NIR FDA UDI
- Description
- VEQTRON ICG/NIR 4K Twinlight LED-Laser Light Source FDA UDI
Identifiers
- Catalog Number
- 71-182-30 NIR FDA UDI
- Primary DI / UDI-DI
- 04250942104519 FDA UDI
- FDA Product Code
- GCJ FDA UDIIZI FDA UDI
- GMDN Term
- Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI892.1600 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Amnotec by AMNOTEC International Medical GmbH — 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 |
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Manufacturer
- Manufacturer
- AMNOTEC International Medical GmbH
Sources (1)
- FDA UDI dd9ce57b-f64c-415b-b7b3-59b5132f147a 35 fields · synced May 30, 2026