DRAP REGISTERED MEDICAL DEVICE
Heartrail II (Guiding Catheter) is registered with DRAP under number MDIR-0003569 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. It is listed as valid until 7 Jun 2027.
Screening result
i
Imported device, registered with DRAP as Class D (high risk)
MDIR-0003569 · the class is taken from DRAP's list for this number
MDIR-0003569 · the class is taken from DRAP's list for this number
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 7 Jun 2027
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Holder has a DRAP import licence on file
ELI-00034
ELI-00034
| Device | Heartrail II (Guiding 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, 150 maimaigi-cho, fujinomiya city, shizuoka prefecture, 418-0015m Japan |
| Issued | 7 Jul 2022 |
| Renewal date | 7 Jun 2027 |
| Licence | ELI-00034 |
Specifications
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Screened 6 Oct 2026, 18:37 (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.