CORDIS Long Sheath.
Class D (high risk) · MDIR-0003938 · Global Marketing Services
DRAP REGISTERED MEDICAL DEVICE
CORDIS Long Sheath. (Long Sheath Set) [501-610, 501-611, 501-612, 501-613, 501-611A, 601-613A, 501-616A, 501-617] is registered with DRAP under number MDIR-0003938 as a Class D (high risk) medical device, imported. The listed holder is Global Marketing Services. It is listed as valid until 6 Nov 2027.
Screening result
MDIR-0003938 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00109
| Device | CORDIS Long Sheath. (Long Sheath Set) [501-610, 501-611, 501-612, 501-613, 501-611A, 601-613A, 501-616A, 501-617] |
|---|---|
| Class | D |
| Listed holder | Global Marketing Services |
| Holder address | 111-B, Hali Road, Westridge 1, Rawalpindi. |
| Manufacturing site | M/s Cordis Corporation 14201 Northwest 60th Avenue Miami Lakes, FL 33014 786.313.2000, USA M/s Cardinal Health Mexico 244 S de RL de CV Santiago Troncoso # 808 Parque Industrial Salvarcar Ciudad Juarez, Chihuahua CP 32574, Mexico |
| Issued | 7 Nov 2022 |
| Renewal date | 6 Nov 2027 |
| Licence | ELI-00109 |
Specifications
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Screened 7 Oct 2026, 06:09 (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.