DRAP REGISTERED MEDICAL DEVICE
Radifoucus Glidewire Advantage (Glidewire catheter) is registered with DRAP under number MDIR-0002793 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. Its listed renewal date (29 Aug 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002793 · 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 | Radifoucus Glidewire Advantage (Glidewire catheter) |
|---|---|
| Class | D |
| Listed holder | Intek Corporation |
| Holder address | Office No 30, First Floor Al Amin Plaza, The Mall Rawalpindi. |
| Manufacturing site | M/s TERUMO CORPORATION 44-1, 2-Chome, Hatagaya, Shibuya-Ku, Tokyo 151-0072 JAPAN M/s Terumo corporation ashitaka factory Address: 150, Maimaigi-Cho, Fujinomiya City, Shizuoka Prefecture 418-0015, Japan |
| Issued | 30 Aug 2021 |
| Renewal date | 29 Aug 2026 |
| Licence | ELI-00034 |
Specifications
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Screened 6 Oct 2026, 01:00 (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 |
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.