Identity
- Trade Name
- Socrates FDA UDI
- Generic Name
- Thrombectomy suction catheter FDA UDI
- Device Name
- Socrates Aspiration System: 156cm working length aspiration catheter FDA UDI
- Model / Reference
- SC038-156-001 FDA UDI
- Description
- Socrates Aspiration System: 156cm working length aspiration catheter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00818075010776 FDA UDI
- 510(k) Number
- K223913 FDA UDI
- FDA Product Code
- NRY FDA UDI
- GMDN Term
- Thrombectomy suction catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 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
No
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Catheter Inner Diameter — 0.038 Inch FDA UDICatheter Working Length — 156 Centimeter FDA UDIOuter Diameter — 1.35 Millimeter FDA UDIOuter Diameter — 0.053 Inch FDA UDICatheter Inner Diameter — 0.97 Millimeter FDA UDICatheter Gauge — 4.0 French FDA UDI
Category: Thrombectomy suction catheter
Socrates by Scientia Vascular, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Thrombectomy suction catheter.
- Symphony™ ProHelix™ — IMPERATIVE CARE INC. · Class II
- Prodigy™ Catheter — IMPERATIVE CARE INC. · Class II
- Symphony™ Advance™ Long Dilator — IMPERATIVE CARE INC. · Class II
- Indigo System — PENUMBRA, INC. · Class II
- Penumbra System — PENUMBRA, INC. · Class II
- Trevo — Stryker Corp.
- Penumbra System — PENUMBRA, INC. · Class II
- Pounce ™ Thrombectomy — Surmodics, Inc. · Class II
Cleared under the same submission
K223913 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Scientia Vascular, Inc.
Sources (1)
- FDA UDI 9d606e99-d97c-46a4-959d-36b770841ddf 37 fields · synced May 30, 2026