DEVICE: All Soft Ureteral Stent - 7F, 24cm with Suture (00812261010694)
Device Identifier (DI) Information
All Soft Ureteral Stent - 7F, 24cm with Suture
7F, 24cm with Suture
In Commercial Distribution
SOT 7/24-S
ALLWIN MEDICAL DEVICES, INC.
7F, 24cm with Suture
In Commercial Distribution
SOT 7/24-S
ALLWIN MEDICAL DEVICES, INC.
7F, 24cm with Suture
Device Characteristics
Labeling does not contain MRI Safety Information | |
Yes | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
58005 | 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.
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Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
FAD | Stent, Ureteral |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K190659 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
8ccde8dd-88a8-49fb-88c0-50eaea481652
September 29, 2020
1
September 21, 2020
September 29, 2020
1
September 21, 2020
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
10812261010691 | 10 | 00812261010694 | In Commercial Distribution |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
714-572-1709
info@allwinmedical.com
info@allwinmedical.com