DRAP REGISTERED MEDICAL DEVICE
Radifocus Guide Wire M is registered with DRAP under number MDIR-0002430 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. Its listed renewal date (31 Mar 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002430 · 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 | Radifocus Guide Wire M |
|---|---|
| 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 Terumo Europe N.V. Interleuvenlaan 40 3001 Leuven Belgium M/s Terumo Corporation Ashitaka Factory 150 Maimaigi-cho, Fujinomiya City, Shizuoka Prefecture 418-0015, Japan M/s Terumo Vietnam Co., Ltd Lot 44a44b-44c Quang Minh Industrial Zone, Me Linh District, Hanoi City, Vietnam |
| Issued | 1 Apr 2021 |
| Renewal date | 31 Mar 2026 |
| Licence | ELI-00034 |
Specifications
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Screened 6 Oct 2026, 20:43 (Pakistan time). A screening aid, not an official DRAP verification.
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| 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.