DRAP REGISTERED MEDICAL DEVICE
Shunmei Micro Catheter (Micro Catheter) is registered with DRAP under number MDIR-0007314 as a Class D (high risk) medical device, imported. The listed holder is Ham International. It is listed as valid until 15 Sep 2029.
Screening result
i
Number type: imported, registered (Class B, C or D)
MDIR-0007314
MDIR-0007314
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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 15 Sep 2029
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Holder has a DRAP import licence on file
ELI-00008
ELI-00008
| Device | Shunmei Micro Catheter (Micro Catheter) |
|---|---|
| Class | D |
| Listed holder | Ham International |
| Holder address | Mezzenine Floor Plot No. LS-2, St,9 Block-15 KDA Scheme, 36 Gulistan-e-Johar, Karachi |
| Manufacturing site | M/s Shunmei Medical Co., Ltd., R401 of building B No. 8 Jinlong Yifa 3rd road, Yifa Industrial Zone Dushi village, Pingtan town, Huiyang District, Huizhou, Guangdong, China |
| Issued | 16 Sep 2024 |
| Renewal date | 15 Sep 2029 |
| Licence | ELI-00008 |
Specifications
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Screened 5 Oct 2026, 07:42 (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.
| MDIE-0000420 | SHUNMEI TR-Closure Band | Class A |
| MDIR-0000904 | Shunmei PTFE Coated Guide Wire | Class D |
| MDIR-0002812 | Shunmei Hemostasis Valve Set | Class B |
| MDIR-0002846 | Shunmei PTCA Balloon Dilatation Catheter | Class D |
| MDIR-0002847 | Shunmei Hydrophilic coated Guide Wire | Class D |
| MDIR-0002848 | Shunmei PTCA Guide Wire | Class D |
| MDIR-0002849 | Shunmei Angiographic Catheter | Class D |
| MDIR-0002850 | Shunmei NC Coronary Dilatation Catheter | Class D |
| MDIR-0002921 | Shunmei Manifolds | Class B |
| MDIR-0003252 | SHUNMEI Guiding Catheter | Class D |
| MDIR-0003659 | SHUNMEI Manifold Kit | Class C |
| MDIR-0007312 | Shunmei Peripheral Guidewire (Peripheral Guidewire) | Class D |
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.
