DRAP REGISTERED MEDICAL DEVICE
HANAROSTENT Biliary (NC) is registered with DRAP under number MDIR-0007168 as a Class C (moderate to high risk) medical device, imported. The listed holder is Meditron Medical Systems. It is listed as valid until 7 Oct 2029.
Screening result
i
Number type: imported, registered (Class B, C or D)
MDIR-0007168
MDIR-0007168
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 7 Oct 2029
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Holder has a DRAP import licence on file
ELI-00295
ELI-00295
| Device | HANAROSTENT Biliary (NC) |
|---|---|
| Class | C |
| Listed holder | Meditron Medical Systems |
| Holder address | 88-A/369-E, Johar Town Lahore |
| Manufacturing site | M/s. M.I Tech Co., Ltd No.174, Habuk 2-gil, Jinwi-myeon, Pyeongtaek-si, Gyeonggi-do, 17706, Republic of Korea |
| Issued | 8 Oct 2024 |
| Renewal date | 7 Oct 2029 |
| Licence | ELI-00295 |
Specifications
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Screened 5 Oct 2026, 00:58 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
Other DRAP registrations and enlistments listed for the same company.
| MDIR-0005814 | Micro-Tech (Esophageal stent) | Class C |
| MDIR-0005815 | Micro-Tech Biliary Drainage Catheter Introducer System | Class B |
| MDIR-0005816 | Micro-Tech Biliary Stent | Class C |
| MDIR-0005817 | Micro-Tech Sterile Biliary Stone Retrieval Balloon Catheter | Class B |
| MDIR-0005818 | Micro-Tech Sterile Hot Snare | Class C |
| MDIR-0005819 | Micro-Tech Tracheal Stent | Class C |
| MDIR-0005820 | Micro-Tech Non Vascular Sterile Hydro Slide Guidewire | Class B |
| MDIR-0005821 | Micro-Tech Intestinal Stent | Class C |
| MDIR-0005822 | Micro-Tech Sterile Sphincterotome | Class C |
| MDIR-0005823 | Micro-Tech Sterile Repositionable Hemostasis Clipping device | Class B |
| MDIR-0006554 | Endoscopic Ultrasound Aspiration Needles (Endoscopic Ultrasound Aspiration Needles) | Class B |
| MDIR-0007169 | CHOOSTNET Colon/Rectum Asymmetric (CCC) | Class C |
Corrections
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Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.