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MEDRAD® Spectris Solaris MRI Integral "T" with Check Valve
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- MEDRAD® Spectris Solaris MRI Integral "T" with Check Valve FDA UDI
- Generic Name
- Angiographic syringe FDA UDI
- Device Name
- 96" low pressure connector tube with T-connector and check valve for Spectris Solaris (MR - 96" T-CONNECT TUBING W/CHECK VALVE) (60728974) FDA UDI
- Model / Reference
- SSIT 96VLD FDA UDI
- Description
- 96" low pressure connector tube with T-connector and check valve for Spectris Solaris (MR - 96" T-CONNECT TUBING W/CHECK VALVE) (60728974) FDA UDI
Identifiers
- Catalog Number
- SSIT 96VLD FDA UDI
- Primary DI / UDI-DI
- 00616258005454 FDA UDI
- FDA Product Code
- DXT FDA UDI
- GMDN Term
- Angiographic syringe 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Angiographic syringe
MEDRAD® Spectris Solaris MRI Integral "T" with Check Valve by Bayer Medical Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 6168ce90-7b27-4a0d-ab09-7101f60bd2b0 35 fields · synced Jun 9, 2026