Identity
- Trade Name
- THRUPORT SYSTEMS ENDOVENT PULMONARY CATHETER KIT FDA UDI
- Generic Name
- Chamber-decompression cardiac catheter FDA UDI
- Device Name
- ENDOVENT PULMONARY CATHETER KIT FDA UDI
- Model / Reference
- EV FDA UDI
- Description
- ENDOVENT PULMONARY CATHETER KIT FDA UDI
Identifiers
- Catalog Number
- EV FDA UDI
- Primary DI / UDI-DI
- 00690103182866 FDA UDI
- 510(k) Number
- K981009 FDA UDI
- FDA Product Code
- DWF FDA UDI
- GMDN Term
- Chamber-decompression cardiac catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4210 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: Chamber-decompression cardiac catheter
Thruport Systems Endovent Pulmonary Catheter Kit by Edwards Lifesciences LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Chamber-decompression cardiac catheter.
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- Edwards Lifesciences Vent Catheter — Edwards Lifesciences LLC · Class II
- Edwards Lifesciences Vent Catheter — Edwards Lifesciences LLC · Class II
- Edwards Lifesciences Vent Catheter — Edwards Lifesciences LLC · Class II
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
- Edwards Lifesciences LLC
Sources (1)
- FDA UDI 40d9ff13-1ead-4edd-98ff-899f6fa8f406 38 fields · synced Jun 8, 2026