REEF HP
- Primary DI
- 08033477048734
- Brand
- REEF HP
- Company
- MEDTRONIC, INC.
- Model
- REE080060082
- Device description
- Cath REE080060082 REEUS 08.00 L060UL0800
- Published
- 2016-06-19
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| DQY | CATHETER, PERCUTANEOUS |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| DQY | Catheter, Percutaneous | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 08033477048734 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 08033477048734 | 08033477048734 | 8033477048734 |
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 |
|---|
| Length | 60 | Millimeter |
| Outer Diameter | 8 | Millimeter |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | Store at controlled room temperature, in a dry place. Keep away from sunlight. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
Regulatory Flags
- DUNS number
- 006261481
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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| 30841156103983 | SUPERCROSS | TELEFLEX INCORPORATED | DQY | 2026-03-23 |
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| 20801902195429 | ARROW | TELEFLEX INCORPORATED | DQY | 2026-03-17 |
| 00857545008394 | Zebra | Q'APEL MEDICAL LLC | DQY | 2026-03-05 |
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