Identity
- Trade Name
- InThrill Thrombectomy Catheter FDA UDI
- Generic Name
- Electronic occlusion spectacles FDA UDI
- Device Name
- InThrill Thrombectomy Catheter (AS-01312) FDA UDI
- Model / Reference
- 43-102 FDA UDI
- Description
- InThrill Thrombectomy Catheter (AS-01312) FDA UDI
Identifiers
- Catalog Number
- 43-102 FDA UDI
- Primary DI / UDI-DI
- 00810123710126 FDA UDI
- 510(k) Number
- K250421 FDA UDI
- FDA Product Code
- QEW FDA UDI
- GMDN Term
- Electronic occlusion spectacles FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5150 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
Yes
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
Category: Electronic occlusion spectacles
InThrill Thrombectomy Catheter by Inari Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K250421 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 |
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Manufacturer
- Manufacturer
- Inari Medical, Inc.
Sources (1)
- FDA UDI 9a8ea348-3729-4e97-bbf6-1c965cc79f0c 36 fields · synced Jun 8, 2026