Identity
- Trade Name
- AMNOTEC FDA UDI
- Generic Name
- Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
- Device Name
- VEQTRON ICG/NIR Cold Light Cable, Ø 4.5 mm, L. 300 cm, Autoclavable FDA UDI
- Model / Reference
- 71-146-30 NIR C-US FDA UDI
- Description
- VEQTRON ICG/NIR Cold Light Cable, Ø 4.5 mm, L. 300 cm, Autoclavable FDA UDI
Identifiers
- Catalog Number
- 71-146-30 NIR C-US FDA UDI
- Primary DI / UDI-DI
- 04250942120601 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
Dry Heat Sterilization 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 067e6b5c-e9df-48f3-943c-e67b70f8d8cf 35 fields · synced May 30, 2026