Identity
- Trade Name
- Armada FDA UDI
- Generic Name
- Peripheral angioplasty balloon catheter, basic FDA UDI
- Device Name
- Armada 18 PTA Catheter 2.5 mm x 40 mm x 150 cm / Over-The-Wire FDA UDI
- Model / Reference
- 1013464-040 FDA UDI
- Description
- Armada 18 PTA Catheter 2.5 mm x 40 mm x 150 cm / Over-The-Wire FDA UDI
Identifiers
- Catalog Number
- 1013464-040 FDA UDI
- Primary DI / UDI-DI
- 08717648207778 FDA UDI
- FDA Product Code
- LIT FDA UDI
- GMDN Term
- Peripheral angioplasty balloon catheter, basic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Peripheral angioplasty balloon catheter, basic
Introducing the Armada, a high-quality peripheral angioplasty balloon catheter designed for safe and effective treatment of stenotic peripheral arteries. With its advanced features and robust design, this device is ideal for clinicians seeking to improve patient outcomes.
Similar devices
Also classified as Peripheral angioplasty balloon catheter, basic.
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- RapidCross — Covidien LP · 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
- Abbott Vascular
Sources (1)
- FDA UDI 2fa53b76-ea14-4c69-8259-76c8cb27ff23 36 fields · synced Jul 24, 2026