Siemens Immulite 1000 Toxoplasma Quantitative IgG Assay kit - DRAP MDIR-0001547 (Class C)

DRAP REGISTERED MEDICAL DEVICE

Siemens Immulite 1000 Toxoplasma Quantitative IgG Assay kit is registered with DRAP under number MDIR-0001547 as a Class C (moderate to high risk) medical device, imported. The listed holder is Hoora Pharma (Pvt) Ltd. Its listed renewal date (10 Jun 2025) has passed, so ask the supplier for the renewal letter.

Screening result

i
Number type: imported, registered (Class B, C or D)
MDIR-0001547
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
!
Renewal date passed on 10 Jun 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
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Holder has a DRAP import licence on file
ELI-00037
DeviceSiemens Immulite 1000 Toxoplasma Quantitative IgG Assay kit
ClassC
Listed holderHoora Pharma (Pvt) Ltd
Holder addressWH-01 20-A7-A8, Korangi Creek Industrial Park, Karachi.
Manufacturing siteM/s Siemens Healthcare Diagnostics Products Limited Glyn Rhonwy, Llanberis, Caernarfon, LL55 4EL, UK
Issued11 Jun 2020
Renewal date10 Jun 2025
LicenceELI-00037

Specifications

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Screened 5 Oct 2026, 01:41 (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.