Mariner
- Primary DI
- 15051684016186
- Brand
- Mariner
- Company
- ANGIODYNAMICS, INC.
- Model
- 11709232
- Device description
- Mariner Angiographic Catheter, Sos Omni Selective (3), Non-Braided
- Published
- 2019-04-29
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| DQO | CATHETER, INTRAVASCULAR, DIAGNOSTIC |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| DQO | Catheter, Intravascular, Diagnostic | Cardiovascular | 2 |
Premarket Submissions
| Submission | Supplement |
|---|---|
| K173762 | 000 |
Premarket Details
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| H787117092320 | Primary | HIBCC | 0 | |
| 15051684016186 | Secondary | GS1 | 0 |
GMDN Terms
| Term | Definition |
|---|---|
| Angiographic catheter, single-use | A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Outer Diameter | 1.8 | Millimeter |
Storage And Handling
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 | 27 Degrees Celsius |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(518)795-1676 | dgreer@angiodynamics.com |
Regulatory Flags
- DUNS number
- 079105071
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company
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|---|---|---|---|---|
| 25051684011713 | AngioDynamics | H787065200010 | 06520001 | 2025-11-14 |
| 25051684029985 | BioFlo | H965460320 | 46-032 | 2025-03-18 |
| 25051684029992 | BioFlo | H965460330 | 46-033 | 2025-03-18 |
| 25051684030004 | BioFlo | H965460420 | 46-042 | 2025-03-18 |
| 25051684030011 | BioFlo | H965460430 | 46-043 | 2025-03-18 |
| 25051684009659 | Soft-Vu | H787107320020 | 10732002 | 2025-03-03 |
| 25051684009642 | Soft-Vu | H787107320010 | 10732001 | 2025-02-27 |
| 15051684016858 | BioFlo Vortex | CT50STBANFVI | 2024-11-19 | |
| 15051684016865 | BioFlo Vortex | CT50STBAVI | 2024-11-19 | |
| 15051684019019 | ADx Guidewire | 810138260 | 2024-11-11 | |
| H7878101351500 | ADx | 810135150 | 2021-01-06 | |
| H7878101352600 | ADx | 810135260 | 2021-01-13 | |
| H7878101381500 | ADx | 810138150 | 2021-01-13 | |
| H7878105251500 | ADx | 810525150 | 2021-01-13 | |
| H7878105252600 | ADx | 810525260 | 2021-01-06 | |
| H7878105321500 | ADx | 810532150 | 2021-01-06 | |
| H7878105350800 | ADx | 810535080 | 2021-01-06 | |
| H7878105351500 | ADx | 810535150 | 2020-11-25 | |
| H7878105351800 | ADx | 810535180 | 2020-11-25 | |
| H7878105352600 | ADx | 810535260 | 2020-11-25 |
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