FDA Registration
Active
🇺🇸 United States
MEDICAL MURRAY, INC.
Reg #: 1424778
·
FEI: 3003473227
·
Expires 2026
Products
7
Proprietary Names
7
Establishment Types
1
Classifications
7
Registration Details
- Registration Name
- MEDICAL MURRAY, INC.
- Registration Number
- 1424778
- FEI Number
- 3003473227
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 540 Capital Drive, Suite 150
- City
- Lake Zurich
- State
- IL
- ZIP
- 60047
- Country
- US
Owner / Operator
- Firm Name
- MURRAY, INC.
- Operator Number
- 9046685
- Address
- 400 N. RAND ROAD, --
- City
- North Barrington
- State
- IL
- Postal Code
- 60010
- Country
- US
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days | LJS | Class 2 | General Hospital | No | 2025-03-03 |
| Stent, Carotid | NIM | Class 3 | Unknown | No | 2024-11-12 |
| Peripheral Mechanical Thrombectomy With Aspiration | QEW | Class 2 | Cardiovascular | No | 2023-10-25 |
| Stent, Ureteral | FAD | Class 2 | Gastroenterology, Urology | No | 2024-11-01 |
| Aortic Stent | PNF | Class 3 | Unknown | No | 2024-09-04 |
| Device, Vascular, For Promoting Embolization | KRD | Class 2 | Cardiovascular | No | 2018-04-10 |
| Catheter, Intravascular Occluding, Temporary | MJN | Class 2 | Cardiovascular | No | 2014-11-20 |
Proprietary Names
Neonav ECG Tip Location System
Neuroguard IEP® 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection
iSweep 14F
RELIEF Ureteral Stent Kit
Minima; Minima Growth Stent; Minima Stent; Minima Stent System; Minima System
Endoluminal Occlusion System (EOS)
RenovoCath RC120 catheter
Establishment Types
Manufacture Medical Device for Another Party (Contract Manufacturer)