DRAP REGISTERED MEDICAL DEVICE
Angiomed PERCUTANEOUS KIDNEY DRAINAGE is registered with DRAP under number MDIR-0002002 as a Class C (moderate to high risk) medical device, imported. The listed holder is Surgi World. Its listed renewal date (6 Dec 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002002
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-00212
| Device | Angiomed PERCUTANEOUS KIDNEY DRAINAGE |
|---|---|
| Class | C |
| Listed holder | Surgi World |
| Holder address | 303, Muhammadia Plaza, College Road, Rawalpindi |
| Manufacturing site | M/s Angiomed GmbH & Co. Medizintechnik KG, Wachausstrasse 6, 76227 Karlsruhe, Germany |
| Issued | 7 Dec 2020 |
| Renewal date | 6 Dec 2025 |
| Licence | ELI-00212 |
Specifications
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Screened 5 Oct 2026, 08:56 (Pakistan time). A screening aid, not an official DRAP verification.
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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.
