DRAP REGISTERED MEDICAL DEVICE
G-TEC Sclerotherapy Needles is registered with DRAP under number MDIR-0009106 as a Class B (low to moderate risk) medical device, imported. The listed holder is Kain Medical. It is listed as valid until 20 Apr 2030.
Screening result
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Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0009106 · the class is taken from DRAP's list for this number
MDIR-0009106 · the class is taken from DRAP's list for this number
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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 20 Apr 2030
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Holder has a DRAP import licence on file
ELI-00506
ELI-00506
| Device | G-TEC Sclerotherapy Needles |
|---|---|
| Class | B |
| Listed holder | Kain Medical |
| Holder address | Ali, Office No. 35, 3rd Floor, Plot No.233-A, Bhai Center, PECHS Block No. 2, Karachi |
| Manufacturing site | M/s Zhejiang Chuangxiang Medical Technology Co., Ltd. Room 101, 201, 301, 401, 501, Building 50 No.650 Hongfeng Road Donghu Street, Yuhang District, Hangzhou City, Zhejiang Province 311100, P.R. China |
| Issued | 21 Apr 2025 |
| Renewal date | 20 Apr 2030 |
| Licence | ELI-00506 |
Specifications
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Screened 6 Oct 2026, 08:32 (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-0007742 | Tek Lens II (Intraocular Lens) [811, 811Y] | Class C |
| MDIR-0008129 | G-TEC Single Use Guidewire | Class B |
| MDIR-0008130 | G-TEC Single Use Grasping Forcep | Class B |
| MDIR-0008131 | G-TEC Single Use Balloon Dilatation Catheter | Class B |
| MDIR-0008132 | G-TEC Single Use Biopsy Forcep | Class B |
| MDIR-0008133 | G-TEC Single Use Hemoclip | Class B |
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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.