| Primary Device ID | 08806367081070 |
| NIH Device Record Key | 06980225-9a5a-4839-bf74-6400a2b0c05c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HANAROSTENT® LowAxTM Duodenum/Pylorus(NNN) |
| Version Model Number | DNJF-20-060-140 |
| Company DUNS | 688454359 |
| Company Name | M.I.Tech Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com | |
| Phone | +821042945040 |
| skim@mitechglobal.com |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Length | 1400 Millimeter |
| Stent Length | 60 Millimeter |
| Stent Diameter | 20 Millimeter |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Storage Environment Temperature | Between 15 Degrees Celsius and 35 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08806367081070 [Primary] |
| MUM | Stent, Metallic, Expandable, Duodenal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2026-01-05 |
| Device Publish Date | 2019-02-18 |
| 08806367081346 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081315 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081285 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081278 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081247 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081216 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081209 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081179 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081148 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081131 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081100 | Un-covered self-expanding nitinol duodenum stent |
| 08806367081070 | Un-covered self-expanding nitinol duodenum stent |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HANAROSTENT 79343425 not registered Live/Pending |
M.I.Tech Co.,Inc 2022-05-31 |
![]() HANAROSTENT 79078614 3903217 Live/Registered |
M.I.Tech Co.,Inc 2009-09-22 |