Identity
- Trade Name
- CABLE,HANDSWITCH,20',DCU,UDI,BATCH FDA UDI
- Generic Name
- CT contrast medium injection system, line-powered, mobile FDA UDI
- Device Name
- CABLE,HANDSWITCH,20',DCU,UDI,BATCH (85594389) FDA UDI
- Model / Reference
- EDS 700 20 FDA UDI
- Description
- CABLE,HANDSWITCH,20',DCU,UDI,BATCH (85594389) FDA UDI
Identifiers
- Catalog Number
- EDS 700 20 FDA UDI
- Primary DI / UDI-DI
- 00616258010519 FDA UDI
- 510(k) Number
- K993728 FDA UDI
- FDA Product Code
- DXT FDA UDI
- GMDN Term
- CT contrast medium injection system, line-powered, mobile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1650 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
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
No
FDA UDI
Category: CT contrast medium injection system, line-powered, mobile
Cable, Handswitch, 20', Dcu, Udi, Batch by Bayer Medical Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Bayer Medical Care Inc.
Sources (1)
- FDA UDI 5b376ab0-fee6-4ed6-aba2-50f9ff9769ec 36 fields · synced Jun 9, 2026