Identity
- Trade Name
- COBRA-OS™ FDA UDI
- Generic Name
- Intravascular occluding balloon catheter, image-guided FDA UDI
- Device Name
- The COBRA-OS™ is intended for temporary occlusion of large vessels including patients requiring emergency control of hemorrhage. FDA UDI
- Model / Reference
- F01K1 FDA UDI
- Description
- The COBRA-OS™ is intended for temporary occlusion of large vessels including patients requiring emergency control of hemorrhage. FDA UDI
Identifiers
- Catalog Number
- F01K1 FDA UDI
- Primary DI / UDI-DI
- 16286780610009 FDA UDI
- 510(k) Number
- K201652 FDA UDI
- FDA Product Code
- MJN FDA UDI
- GMDN Term
- Intravascular occluding balloon catheter, image-guided FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4450 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
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
Yes
FDA UDI
Cobra-Os™ by Front Line Medical Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Front Line Medical Technologies Inc.
Sources (1)
- FDA UDI aac28ef7-1225-4e6e-8319-d416d1a8dea5 36 fields · synced May 30, 2026