Gusta
Class D (high risk) · MDIR-0006314 · Intek Corporation
DRAP REGISTERED MEDICAL DEVICE
Gusta (PTCA NC Balloon Dilatation Catheter) is registered with DRAP under number MDIR-0006314 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. It is listed as valid until 21 Feb 2029.
Screening result
MDIR-0006314 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00034
| Device | Gusta (PTCA NC Balloon Dilatation Catheter) |
|---|---|
| Class | D |
| Listed holder | Intek Corporation |
| Holder address | Office. 517, Kohistan Towers, Mehfooz Road, Saddar, Rawalpindi. |
| Manufacturing site | M/s Beijing Demax Medical Technology Co., Ltd A13-7, Jingshengnansi Street, Tongzhou District, 101102 Beijing, People's Republic of China |
| Issued | 22 Feb 2024 |
| Renewal date | 21 Feb 2029 |
| Licence | ELI-00034 |
Specifications
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Screened 7 Oct 2026, 00:04 (Pakistan time). A screening aid, not an official DRAP verification.
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Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
| MDIR-0005687 | Gusta PTCA Balloon Dilatation Catheter | Class D | Intek Coporation (Pvt) Ltd. |
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.