DRAP REGISTERED MEDICAL DEVICE
SOFIA PLUS Percutaneous Catheter (Distal Access + Aspiration) is registered with DRAP under number MDIR-0001141 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. Its listed renewal date (25 Dec 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001141 · 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 | SOFIA PLUS Percutaneous Catheter (Distal Access + Aspiration) |
|---|---|
| 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 Microvention Europe 30 bis rue du Vieli Abreuvior, 78100 Saint Germain e Laye, France M/s MicroVension,Inc 1311 Valencia Avenue Tustin, California, 92780 USA M/s MicroVension Inc 35 Enterprise, Aliso Viejo, CA 92656, USA M/s MicroVension Costa Rica S.R.L Edificio B33 Zona Franca Coyol Alajuela, Costa Rica |
| Issued | 26 Dec 2019 |
| Renewal date | 25 Dec 2024 |
| Licence | ELI-00034 |
Specifications
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Screened 5 Oct 2026, 13:18 (Pakistan time). A screening aid, not an official DRAP verification.
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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.