POWERFLEX
- Primary DI
- 20705032004371
- Brand
- POWERFLEX
- Company
- CORDIS CORPORATION
- Model
- 4206020S
- Catalog number
- 4206020S
- Device description
- POWERFLEX P3 F5 6X2 80
- Published
- 2016-08-01
- 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 |
|---|---|
| DQY | CATHETER, PERCUTANEOUS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DQY | Catheter, Percutaneous | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K032737 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20705032004371 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20705032004371 | 20705032004371 |
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 microsurgical blades (atherotomes) to score the plaque. This is a single-use device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Do not use if package is damanged |
| Special Storage Condition, Specify | 0 | 0 | Keep away from sunlight |
| Special Storage Condition, Specify | 0 | 0 | Keep dry |
| Storage Environment Temperature | 15 Degrees Celsius | 30 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 806136177
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
- No natural rubber latex
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10705032000512 | AVANTI+ | 402604T | 402604T | 2016-08-01 |
| 10705032000550 | AVANTI | 402605R | 402605R | 2016-08-01 |
| 10705032000772 | AVANTI+ | 402611T | 402611T | 2016-08-01 |
| 10705032009751 | AVANTI | 504404X | 504404X | 2016-08-01 |
| 10705032009782 | AVANTI | 504407X | 504407X | 2016-08-01 |
| 10705032009805 | AVANTI | 504409X | 504409X | 2016-08-01 |
| 10705032009812 | AVANTI | 504504S | 504504S | 2016-08-01 |
| 10705032009829 | AVANTI | 504505S | 504505S | 2016-08-01 |
| 10705032009836 | AVANTI | 504505X | 504505X | 2016-08-01 |
| 10705032009843 | AVANTI | 504506S | 504506S | 2016-08-01 |
| 10705032009850 | AVANTI | 504506X | 504506X | 2016-08-01 |
| 10705032009867 | AVANTI | 504507X | 504507X | 2016-08-01 |
| 10705032009874 | AVANTI | 504508X | 504508X | 2016-08-01 |
| 10705032009928 | AVANTI | 504604T | 504604T | 2016-08-01 |
| 10705032009973 | AVANTI | 504605T | 504605T | 2016-08-01 |
| 10705032010009 | AVANTI | 504606D | 504606D | 2016-08-01 |
| 10705032010016 | AVANTI | 504606P | 504606P | 2016-08-01 |
| 10705032010023 | AVANTI | 504606S | 504606S | 2016-08-01 |
| 10705032010030 | AVANTI | 504606T | 504606T | 2016-08-01 |
| 10705032010054 | AVANTI | 504606X | 504606X | 2016-08-01 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
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| 06934955914744 | Teleport Glide Microcatheter | OrbusNeich Medical (ShenZhen) Co., Ltd. | DQY | 2026-07-20 |
| 06934955914751 | Teleport Glide Microcatheter | OrbusNeich Medical (ShenZhen) Co., Ltd. | DQY | 2026-07-20 |
| 06934955914768 | Teleport Glide Microcatheter | OrbusNeich Medical (ShenZhen) Co., Ltd. | DQY | 2026-07-20 |
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| 06934955914874 | Teleport Glide Microcatheter | OrbusNeich Medical (ShenZhen) Co., Ltd. | DQY | 2026-07-20 |
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