DRAP REGISTERED MEDICAL DEVICE
Xcess Guiding Catheter is registered with DRAP under number MDIR-0001719 as a Class D (high risk) medical device, imported. The listed holder is Al Waali Care Concepts. Its listed renewal date (18 Aug 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001719 · the class is taken from DRAP's list for this number
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-00386
| Device | Xcess Guiding Catheter |
|---|---|
| Class | D |
| Listed holder | Al Waali Care Concepts |
| Holder address | 86-Allama Iqbal Road, Chah Baba Shadiwal Street, Garhi Shahu, District Lahore |
| Manufacturing site | M/s Curatia Medical Limited 198 Xiangjiang Road New District, Suzhou, Jiangsu, China, 215011 |
| Issued | 19 Aug 2020 |
| Renewal date | 18 Aug 2025 |
| Licence | ELI-00386 |
Specifications
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Screened 6 Oct 2026, 03:41 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
Other DRAP registrations and enlistments listed for the same company.
| MDIR-0002460 | CONIC ONE (PTCA BALLOON CATHETER) | Class D |
| MDIR-0002461 | CLEVER PTCA BALLOON CATHETER | Class D |
| MDIR-0003125 | MILVUS (PTA BALLOON CATHETER) | Class B |
| MDIR-0003126 | MILVUS CONIC (PTA BALLOON CATHETER) | Class B |
| MDIR-0003127 | MILVUS PLUS (PTA BALLOON CATHETER) | Class B |
| MDIR-0003128 | Vela RX PTA Balloon Dilatation Catheter | Class B |
| MDIR-0003215 | KDL Introducer Set (Introducer Set) | Class B |
| MDIR-0003216 | KDL Manifold (Manifold) | Class B |
| MDIR-0003217 | KDL Manifold kit (Manifold) | Class B |
| MDIR-0003218 | KDL Inflation Device | Class B |
| MDIR-0003219 | KDL Guiding catheter | Class D |
| MDIR-0003220 | KDL Angiographic Catheter | Class D |
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.
