NA
- Primary DI
- 20613994885689
- Brand
- NA
- Company
- MEDTRONIC, INC.
- Model
- 007875
- Device description
- WIRE ANG 007875 10PK .035X45 3MMJ SS
- Published
- 2016-09-16
- 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 |
|---|
| DQX | WIRE, GUIDE, CATHETER |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| DQX | Wire, Guide, Catheter | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 20613994885689 | Package | GS1 | 10 | Not in Commercial Distribution |
| 00613994885685 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 20613994885689 | 20613994885689 | | |
| 00613994885685 | 00613994885685 | 613994885685 | 0613994885685 |
GMDN Terms
| Term | Definition |
|---|
| Cardiac/peripheral vascular guidewire, single-use | A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Outer Diameter | 0.889 | Millimeter |
Regulatory Flags
- DUNS number
- 006261481
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- 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
- false
- Sterilization required before use
- false
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| 10816349013598 | GuideRight | Lake Region Medical | DQX | 2026-03-24 |
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| 20801902193418 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-03-23 |
| 20801902221876 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-03-13 |
| 20801902221883 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-03-13 |
| 20801902221890 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-03-13 |
| 20801902225522 | ARROW | TELEFLEX INCORPORATED | DQX | 2026-03-11 |
| 16936733736408 | ULTRASKIN | Lepu Medical Technology (Beijing) Co.,Ltd. | DQX | 2026-02-27 |
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| 16936733736644 | ULTRASKIN | Lepu Medical Technology (Beijing) Co.,Ltd. | DQX | 2026-02-27 |
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| 16936733736965 | ULTRASKIN | Lepu Medical Technology (Beijing) Co.,Ltd. | DQX | 2026-02-27 |
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| 16936733737085 | ULTRASKIN | Lepu Medical Technology (Beijing) Co.,Ltd. | DQX | 2026-02-27 |