Exodus
- Primary DI
- H965105290
- Brand
- Exodus
- Company
- NAVILYST MEDICAL, INC.
- Model
- 10529
- Device description
- Nuance Nephrostomy Drainage Catheter 12F x 35cm with Standard Pigtail
- Published
- 2016-08-03
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FGE | CATHETER, BILIARY, DIAGNOSTIC |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FGE | Stents, Drains And Dilators For The Biliary Ducts | Gastroenterology, Urology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K152069 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| H965105291 | Package | HIBCC | 5 | In Commercial Distribution |
| H965105290 | Primary | HIBCC | 0 | |
| 15051684022743 | Secondary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 15051684022743 | 15051684022743 |
GMDN Terms#
| Term | Definition |
|---|---|
| Nephrostomy catheter | A sterile, flexible tube intended to be inserted percutaneously into the renal pelvis to gain access to the upper urinary tract. This device consists of a large-bore (sizes from 14 to 24 Fr are typical), thin-walled tube usually with a self-retained tip; it sometimes has expanding wings on its tip. It is used to perform drainage for relief of supravesicular obstructions and may also be intended for a variety of procedures of the upper urinary tract including dilation of strictures, removal of calculi, perfusion with chemolytic agents for dissolution of renal stones, or ureteral stenting. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 12 | French |
| Length | 35 | Centimeter |
| Outer Diameter | 4 | Millimeter |
Contacts#
| Phone | |
|---|---|
| +1(518)795-1676 | dgreer@angiodynamics.com |
Regulatory Flags#
- DUNS number
- 809699023
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| H787CT50LPBANFVI0 | BioFlo Vortex | CT50LPBANFVI | 2020-05-29 | |
| H787CT50LPBAVI0 | BioFlo Vortex | CT50LPBAVI | 2020-05-29 | |
| H787CT50LPBDNFVI0 | BioFlo Vortex | CT50LPBDNFVI | 2020-05-29 | |
| H787CT50LPBDVI0 | BioFlo Vortex | CT50LPBDVI | 2020-05-29 | |
| H787CT50LTBANFVI0 | BioFlo Vortex | CT50LTBANFVI | 2020-05-29 | |
| H787CT50LTBAVI0 | BioFlo Vortex | CT50LTBAVI | 2020-05-29 | |
| H787CT50LTBDNFVI0 | BioFlo Vortex | CT50LTBDNFVI | 2020-05-29 | |
| H787CT50LTBDVI0 | BioFlo Vortex | CT50LTBDVI | 2020-05-29 | |
| H787CT50PTBANFVI0 | BioFlo Vortex | CT50PTBANFVI | 2020-05-29 | |
| H787CT50PTBAVI0 | BioFlo Vortex | CT50PTBAVI | 2020-05-29 | |
| H787CT50PTBDNFVI0 | BioFlo Vortex | CT50PTBDNFVI | 2020-05-29 | |
| H787CT50PTBDVI0 | BioFlo Vortex | CT50PTBDVI | 2020-05-29 | |
| H787CT50STBDNFVI0 | BioFlo Vortex | CT50STBDNFVI | 2020-05-29 | |
| H787CT50STBDVI0 | BioFlo Vortex | CT50STBDVI | 2020-05-29 | |
| H787CT60LPBANFVI0 | BioFlo Vortex | CT60LPBANFVI | 2020-05-29 | |
| H787CT60LPBAVI0 | BioFlo Vortex | CT60LPBAVI | 2020-05-29 | |
| H787CT60LPBDNFVI0 | BioFlo Vortex | CT60LPBDNFVI | 2020-05-29 | |
| H787CT60LPBDVI0 | BioFlo Vortex | CT60LPBDVI | 2020-05-29 | |
| H787CT60LPPANFNV0 | BioFlo Vortex | CT60LPPANFNV | 2020-05-29 | |
| H787CT60LPPANFVI0 | BioFlo Vortex | CT60LPPANFVI | 2020-05-29 |
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