Identity
- Trade Name
- Aquarius 8600 FDA UDI
- Generic Name
- Diagnostic x-ray digital imaging conversion system FDA UDI
- Device Name
- Flat Panel Digital Medical X-Ray Imaging Detector - Wireless FDA UDI
- Model / Reference
- 1717WCI FDA UDI
- Description
- Flat Panel Digital Medical X-Ray Imaging Detector - Wireless FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00823073005112 FDA UDI
- 510(k) Number
- K173273 FDA UDI
- FDA Product Code
- MQB FDA UDI
- GMDN Term
- Diagnostic x-ray digital imaging conversion system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1680 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Height — 15.1 Millimeter FDA UDIWidth — 460 Millimeter FDA UDILength — 460 Millimeter FDA UDIWeight — 4.67 Kilogram FDA UDI
Category: Diagnostic x-ray digital imaging conversion system
Aquarius 8600 by Imaging Dynamics Company Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K173273 also covers:
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
- Imaging Dynamics Company Ltd
Sources (1)
- FDA UDI 87b4289a-dc1f-43d0-938d-b53a6a49c42f 37 fields · synced May 30, 2026