DRAP REGISTERED MEDICAL DEVICE
High Flow Diagnostic Catheter is registered with DRAP under number MDIR-0000589 as a Class D (high risk) medical device, imported. The listed holder is Global Marketing Services. Its listed renewal date (16 Jul 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000589
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-00109
| Device | High Flow Diagnostic Catheter |
|---|---|
| Class | D |
| Listed holder | Global Marketing Services |
| Holder address | 111-B, Hali Road, Westridge 1, Rawalpindi., Godown: Same as above |
| Manufacturing site | M/s Cordis Corporation 14201 N.W. 60th Ave. Miami Lakes, FL 33014, USA M/s Cordis de Mexico S.A. de C.V Calle Circuito Interior Norte # 1820, Parque Industrial Salvarcar, Ciudad Juarez, Chihuahua, CP32574, Mexico |
| Issued | 17 Jul 2019 |
| Renewal date | 16 Jul 2024 |
| Licence | ELI-00109 |
Specifications
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Screened 5 Oct 2026, 08:40 (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.
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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.