Identity
- Trade Name
- Smart Coil FDA UDI
- Generic Name
- Vascular microcatheter FDA UDI
- Device Name
- 400SMTSFT3H04 FDA UDI
- Model / Reference
- 400SMTSFT3H04 FDA UDI
- Description
- 400SMTSFT3H04 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00814548016993 FDA UDI
- 510(k) Number
- K143218 FDA UDI
- FDA Product Code
- HCG FDA UDI
- GMDN Term
- Vascular microcatheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5950 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
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Vascular microcatheter
Smart Coil by Penumbra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vascular microcatheter.
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- PROWLER — Medos International Sàrl · Class II
- Merit Maestro® — Merit Medical Systems, Inc. · Class II
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- Direxion™ — Boston Scientific · Class II
- SUPERCROSS — TELEFLEX INCORPORATED · Class II
Cleared under the same submission
K143218 also covers:
- Penumbra System — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
- Smart Coil — PENUMBRA, INC.
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
- Penumbra, Inc.
Sources (1)
- FDA UDI f5424a2d-efda-49d3-8008-546bb1eb5f01 34 fields · synced May 31, 2026