DRAP REGISTERED MEDICAL DEVICE
IMMULITE AFP Sample Diluent IMMULITE 1000 AFP Assay is registered with DRAP under number MDIR-0000961 as a Class C (moderate to high risk) medical device, imported. The listed holder is Hoora Pharma (Pvt) Ltd. Its listed renewal date (28 Nov 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000961
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-00037
| Device | IMMULITE AFP Sample Diluent IMMULITE 1000 AFP Assay |
|---|---|
| Class | C |
| Listed holder | Hoora Pharma (Pvt) Ltd |
| Holder address | WH-01 20-A7-A8, Korangi Creek Industrial Park, Karachi. |
| Manufacturing site | M/s Siemens Healthcare Diagnostics Products Limited Glyn Rhonwy, Llanberis, Caernarfon, LL55 4EL, UK |
| Issued | 29 Nov 2019 |
| Renewal date | 28 Nov 2024 |
| Licence | ELI-00037 |
Specifications
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Screened 5 Oct 2026, 00:51 (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.
