DRAP REGISTERED MEDICAL DEVICE
ANGIOWAY MANIFOLD is registered with DRAP under number MDIR-0003085 as a Class B (low to moderate risk) medical device, imported. The listed holder is Intek Corporation. It is listed as valid until 22 Dec 2026.
Screening result
i
Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0003085 · the class is taken from DRAP's list for this number
MDIR-0003085 · 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 22 Dec 2026
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Holder has a DRAP import licence on file
ELI-00034
ELI-00034
| Device | ANGIOWAY MANIFOLD |
|---|---|
| Class | B |
| Listed holder | Intek Corporation |
| Holder address | Office No 30, First Floor Al Amin Plaza, The Mall Rawalpindi. |
| Manufacturing site | M/s Lepu Medical Technology (Beijing) Co., Ltd., No. 37 Chaoqian Road, Changping District, Beijing, 102200 China |
| Issued | 23 Dec 2021 |
| Renewal date | 22 Dec 2026 |
| Licence | ELI-00034 |
Specifications
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Screened 6 Oct 2026, 17:16 (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.