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Hanarostent®
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref EPB18110-X070Model HANAROSTENT® Esophagus (NCN)
Identity
- Trade Name
- HANAROSTENT® EUDAMEDHANAROSTENT® Esophagus (NCN) FDA UDI
- Generic Name
- Polymer-metal oesophageal stent FDA UDI
- Device Name
- Esophageal Stent with Delivery System EUDAMEDPartially Covered metallic esophagus stent FDA UDI
- Model / Reference
- HANAROSTENT® Esophagus (NCN) EUDAMEDEPB18110-X070 EUDAMEDFDA UDI
- Description
- Partially Covered metallic esophagus stent FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08806367039491 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08806367039491 EUDAMED
- 510(k) Number
- K201160 FDA UDI
- FDA Product Code
- ESW FDA UDI
- EMDN Code
- P050199 ESOPHAGEAL PROSTHESES - OTHER EUDAMED
- GMDN Term
- Polymer-metal oesophageal stent FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.3610 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
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 — 18 Millimeter FDA UDIStent Length — 110 Millimeter FDA UDI
Hanarostent® by M.I.Tech Co., Ltd. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08806367039491 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- M.I.Tech Co., Ltd
- EUDAMED SRN
- KR-MF-000011623
- Authorised Representative
- KTR Europe GmbH DE-AR-000005685
Sources (2)
- EUDAMED 75569d4a-0095-4f69-ac00-b4362f4308c8 61 fields · synced Jul 9, 2026
- FDA UDI ef3d3403-9152-437f-ba45-646a30f8134e 37 fields · synced May 30, 2026