DRAP REGISTERED MEDICAL DEVICE
Occlutech Muscular VSD Occluder is registered with DRAP under number MDIR-0001111 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. Its listed renewal date (22 Dec 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001111 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00034
| Device | Occlutech Muscular VSD Occluder |
|---|---|
| Class | D |
| Listed holder | Intek Corporation |
| Holder address | Office No 30, First Floor Al Amin Plaza, The Mall Rawalpindi., Godown Address: 25 A Nagi Road Westridge 1, Rawalpindi. |
| Manufacturing site | M/s. Occlutech GmbH Winzerlaer Strasse 2 07745 Jena Germany M/s Occlutech Tibbi Urunler San.ve Tic.Ltd.Sti. AHL Serbest Bolgesi, E-5 Blok, 34149, Istanbul Turkey |
| Issued | 23 Dec 2019 |
| Renewal date | 22 Dec 2024 |
| Licence | ELI-00034 |
Specifications
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Screened 6 Oct 2026, 18:11 (Pakistan time). A screening aid, not an official DRAP verification.
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| MDIR-0000247 | ERIC TM Retrieval Device | Class D |
| MDIR-0000383 | MemoPart TM Ventricular Septal Defect (VSD) Occluder | Class D |
| MDIR-0000384 | MemoPart TM Atrial Septal Defect (ASD) Occluder | Class D |
| MDIR-0000385 | MemoPart TM Occluder Delivery System | Class D |
| MDIR-0000386 | MemoPart TM Patent Ductus Arterious (PDA) Occluder | Class D |
| MDIR-0000387 | Figulla Flex II ASD Occluder | Class D |
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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.