Identity
- Trade Name
- Symphony™ Catheter FDA UDI
- Generic Name
- Thrombectomy suction catheter FDA UDI
- Device Name
- 24F Symphony™ Catheter w/ Advance™ Long Dilator FDA UDI
- Model / Reference
- SYMPHONY24F-A FDA UDI
- Description
- 24F Symphony™ Catheter w/ Advance™ Long Dilator FDA UDI
Identifiers
- Catalog Number
- SYMPHONY24F-A FDA UDI
- Primary DI / UDI-DI
- 00850032079136 FDA UDI
- FDA Product Code
- QEW FDA UDIKRA FDA UDI
- GMDN Term
- Thrombectomy suction catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5150 FDA UDI870.1210 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Dimensions & Sizes
- Size
- Introducer Sheath Compatibility — 24 French FDA UDICatheter Working Length — 85 Centimeter FDA UDI
Symphony™ Catheter by Imperative Care Inc. — 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
- Imperative Care Inc.
Sources (1)
- FDA UDI e08f07eb-4f85-4ff3-92a0-6f8fbc96d168 38 fields · synced May 30, 2026