← Back to catalogue
Niti-S Biliary Slim M Stent
FDA UDIFDA 510(k)Class II (US FDA UDI)
510(k) K251123
Identity
- Trade Name
- Niti-S Biliary Slim M Stent FDA UDI
- Generic Name
- Bare-metal biliary stent FDA UDI
- Device Name
- Bare Metal Biliary Stent System FDA UDI
- Model / Reference
- BN0606-6 FDA UDI
- Description
- Bare Metal Biliary Stent System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809744975269 FDA UDI
- 510(k) Number
- K221071 FDA UDI
- FDA Product Code
- FGE FDA UDI
- GMDN Term
- Bare-metal biliary stent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Stent Diameter — 6 Millimeter FDA UDIStent Length — 60 Millimeter FDA UDICatheter Working Length — 180 Centimeter FDA UDICrossing Profile — 6 French FDA UDI
Category: Bare-metal biliary stent
Niti-S Biliary Slim M Stent by Taewoong Medical — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Similar devices
Also classified as Bare-metal biliary stent.
- ALIMAXX-B® — Merit Medical Systems, Inc. · Class II
- PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System — Cordis US Corp. · Class II
- LifeStar® Biliary Stent — Bard Peripheral Vascular · Class II
- SMART FLEX — Cordis US Corp. · Class II
- BONASTENT® Biliary — Sewoon Medical Co., Ltd. · Class II
- Palmaz BLUE Transhepatic Biliary Stent on SLALOM .018 System — Cordis US Corp. · Class II
- Valeo® Balloon Expandable Biliary Stent — Bard Peripheral Vascular · Class II
- E·Luminexx® Biliary Stent — Bard Peripheral Vascular · Class II
Cleared under the same submission
K221071 also covers:
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
- Niti-S Biliary Slim M Stent — Taewoong Medical
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K251123 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Taewoong Medical
- FDA Applicant
- Taewoong Medical Co., Ltd.
Sources (2)
- FDA UDI b32d69fb-50d9-4aa0-9693-6a66e7392873 61 fields · synced Jun 18, 2026
- FDA 510(k) K251123 1 fields · synced Jun 4, 2026