DRAP REGISTERED MEDICAL DEVICE
Destination Carotid Guiding Sheath is registered with DRAP under number MDIR-0001653 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. Its listed renewal date (16 Aug 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001653 · 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 | Destination Carotid Guiding Sheath |
|---|---|
| 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 Medical Corporation 950 Elkton Boulevard, Elkton, Maryland 21921 USA, |
| Issued | 17 Aug 2020 |
| Renewal date | 16 Aug 2025 |
| Licence | ELI-00034 |
Specifications
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Screened 6 Oct 2026, 13:51 (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.