Small Peripheral Cutting Balloon®
- Primary DI
- 08714729819714
- Brand
- Small Peripheral Cutting Balloon®
- Company
- BOSTON SCIENTIFIC CORPORATION
- Model
- M001PCBM4015140F0
- Device description
- Microsurgical Dilatation Device
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| PNO | Catheter, percutaneous, cutting/scoring |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| PNO | Catheter, Percutaneous, Cutting/Scoring | Cardiovascular | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08714729819714 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08714729819714 | 08714729819714 | 8714729819714 |
GMDN Terms#
| Term | Definition |
|---|---|
| Peripheral angioplasty balloon catheter, basic | A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Regulatory Flags#
- DUNS number
- 021717889
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 00802526613876 | LATITUDE® NXT | 6460 | 6460 | 2020-04-09 |
| 08714729893431 | ROTAPRO™ Advancer | H74939299A0 | 2018-07-11 | |
| 08714729999560 | ROTAPRO™ | H749394671250 | H749394671250 | 2020-07-01 |
| 08714729999577 | ROTAPRO™ | H749394671500 | H749394671500 | 2020-07-01 |
| 08714729999584 | ROTAPRO™ | H749394671750 | H749394671750 | 2020-07-01 |
| 08714729999591 | ROTAPRO™ | H749394672000 | H749394672000 | 2020-07-01 |
| 08714729999607 | ROTAPRO™ | H749394672150 | H749394672150 | 2020-07-01 |
| 08714729999614 | ROTAPRO™ | H749394672250 | H749394672250 | 2020-07-01 |
| 08714729999621 | ROTAPRO™ | H749394672380 | H749394672380 | 2020-07-01 |
| 08714729999638 | ROTAPRO™ | H749394672500 | H749394672500 | 2020-07-01 |
| 00191506062620 | RIVOS™ | M00553900 | M00553900 | 2026-06-25 |
| 08714729050650 | Entry Kit | M001503500 | M001503500 | 2016-01-29 |
| 08714729082026 | SteeroCath-Dx™ | M0042028BL0 | 2016-09-24 | |
| 08714729085249 | Electrophysiology Cable | M0049000 | 2016-09-24 | |
| 08714729114659 | Greenfield™ | M001503000 | M001503000 | 2015-09-24 |
| 08714729114666 | Greenfield™ | M001503010 | M001503010 | 2015-09-24 |
| 08714729124993 | Greenfield™ | M001505010 | M001505010 | 2015-09-24 |
| 08714729270249 | Electrophysiology Cable | M004901AS0 | 2016-09-24 | |
| 08714729270256 | Electrophysiology Cable | M004901BS0 | 2016-09-24 | |
| 08714729334996 | Electrophysiology Cable | M004921B0 | 2016-09-24 |
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