GENOSS DES Sirolimus Eluting Coronary Stent System.
Class D (high risk) · MDIR-0002545 · Alliance Medical
DRAP REGISTERED MEDICAL DEVICE
GENOSS DES Sirolimus Eluting Coronary Stent System. is registered with DRAP under number MDIR-0002545 as a Class D (high risk) medical device, imported. The listed holder is Alliance Medical. Its listed renewal date (25 May 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002545 · 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-00147
| Device | GENOSS DES Sirolimus Eluting Coronary Stent System. |
|---|---|
| Class | D |
| Listed holder | Alliance Medical |
| Holder address | 12-B, 1st Floor, Agro Flats, Shadman, Lahore. |
| Manufacturing site | M/s Genoss Co. Ltd. 1F, Gyeonggi R&DB Center, 226, 2F, GSBC, 105, Gwanggyo-ro, Yeongtong-gu, Suwon-si, Gyeonggi-do, Korea. |
| Issued | 26 May 2021 |
| Renewal date | 25 May 2026 |
| Licence | ELI-00147 |
Specifications
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Screened 7 Oct 2026, 00:04 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
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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.