DRAP REGISTERED MEDICAL DEVICE
LIAISON XL MUREX HIV AB/AG HT (REF 310290) & LIAISON Control MUREX HIV AB/AG HT (REF 310291) is registered with DRAP under number MDIR-0006185 as a Class D (high risk) medical device, imported. The listed holder is Sind Medical Stores. It is listed as valid until 30 Jan 2029.
Screening result
MDIR-0006185
DRAP registered Class B/C/D list, 28 Aug 2025
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | LIAISON XL MUREX HIV AB/AG HT (REF 310290) & LIAISON Control MUREX HIV AB/AG HT (REF 310291) |
|---|---|
| Class | D |
| Listed holder | Sind Medical Stores |
| Holder address | 13- B, Block 6, PECHS, Shahrah -e- Faisal Karachi. |
| Manufacturing site | M/s DiaSorin S.P.A., Via Crescentino, snc 13040 Saluggia (VC) - Italy |
| Issued | 31 Jan 2024 |
| Renewal date | 30 Jan 2029 |
Specifications
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Screened 5 Oct 2026, 01:39 (Pakistan time). A screening aid, not an official DRAP verification.
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| MDIR-0002243 | MUREX HBsAg (Version 3) IVD Kit. 9F80-01 (96 Tests), 9F80-05 (480 Tests) | Class D |
| MDIR-0002244 | ICE* Syphilis IVD Kit. 8E04-01 (96 Tests), 8E04-02 (480 Tests) | Class D |
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| MDIR-0002502 | Liaison SARS CoV-2 IgM (Kit) | Class C |
| MDIR-0002726 | AccuPower SARS-CoV-2 Multiplex Real-Time RT-PCR Kit Size: 100 Tests Code: SCVM-2112 | Class C |
| MDIR-0003500 | DemeLene Mesh (Mesh Surgical Polymeric) | Class D |
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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.