MemoPart Snare [Sizes: Snare-15, Snare-20]
Class D (high risk) · MDIR-0003310 · Intek Corporation
DRAP REGISTERED MEDICAL DEVICE
MemoPart Snare [Sizes: Snare-15, Snare-20] is registered with DRAP under number MDIR-0003310 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. It is listed as valid until 14 Mar 2027.
Screening result
MDIR-0003310 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00034
| Device | MemoPart Snare [Sizes: Snare-15, Snare-20] |
|---|---|
| Class | D |
| Listed holder | Intek Corporation |
| Holder address | Office No 30, First Floor Al Amin Plaza, The Mall Rawalpindi. |
| Manufacturing site | M/s Shanghai Shape Memory Alloy Co., Ltd., 1F and 5F, Tower 41, No 258, Xinzhuan Road, Songjiang High-Tech Park, CaoHejing Development District, Shanghai, 201612, China |
| Issued | 15 Mar 2022 |
| Renewal date | 14 Mar 2027 |
| Licence | ELI-00034 |
Specifications
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Screened 7 Oct 2026, 04:52 (Pakistan time). A screening aid, not an official DRAP verification.
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| MDIR-0000385 | MemoPart TM Occluder Delivery System | Class D |
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| MDIR-0000387 | Figulla Flex II ASD Occluder | 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.
