Silhouette® Comfort Ureteral Stent
- Primary DI
- 00607915112318
- Brand
- Silhouette® Comfort Ureteral Stent
- Company
- APPLIED MEDICAL RESOURCES CORPORATION
- Model
- B3834
- Device description
- Temporary indwelling ureteral catheter to assist in urine drainage.
- Published
- 2015-07-13
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| FAD | Stent, Ureteral |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| FAD | Stent, Ureteral | Gastroenterology, Urology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00607915112318 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00607915112318 | 00607915112318 | 607915112318 | 0607915112318 |
GMDN Terms
| Term | Definition |
|---|---|
| Polymeric ureteral stent | A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed ureter (e.g., from stone, stricture, compression, fibrosis, trauma) to maintain luminal patency allowing urine to drain from the renal pelvis to the bladder. It is made of a synthetic polymer(s) [e.g., polytetrafluoroethylene (PTFE), polyethylene (PE), silicone], sometimes with a hydrophilic coating (e.g., hydrogel), and may have various designs (e.g., continuous tube with or without drainage side holes, covered or non-covered mesh structure). Disposable devices intended to assist implantation may be included. The device is typically intended for long-term, but not permanent, implantation. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 4.6 | French |
| Length | 20 | Centimeter |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| 1.949.713.8300 | contact@appliedmedical.com |
Regulatory Flags
- DUNS number
- 187129135
- 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
- true
- Sterilization required before use
- false
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