DRAP REGISTERED MEDICAL DEVICE
MINDRAY Cytomegalovirus IgG (CLIA) is registered with DRAP under number MDIR-0008495 as a Class C (moderate to high risk) medical device, imported. The listed holder is MR Medical Pakistan Pvt Ltd. It is listed as valid until 25 Mar 2030.
Screening result
MDIR-0008495 · the class is taken from DRAP's list for this number
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 | MINDRAY Cytomegalovirus IgG (CLIA) |
|---|---|
| Class | C |
| Listed holder | MR Medical Pakistan Pvt Ltd |
| Holder address | Office No. 1101, 11th Floor, ISE Tower, Jinnah Avenue, Blue Area, Islamabad |
| Manufacturing site | M/s Shenzhen Mindray Bio-Medical Electronics Co., Ltd.Mindray Building, Keji 12th Road South, High-Tech Industrial Park, Nanshan, 518057, Shenzhen, Reople's Republic of China. |
| Issued | 26 Mar 2025 |
| Renewal date | 25 Mar 2030 |
Specifications
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Screened 5 Oct 2026, 12:48 (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.
| MDIE-0001587 | Mindray Chemistry Analyzer [BS 600M] | Class A |
| MDIE-0001588 | Mindray Chemistry Analyzer [BS 240] | Class A |
| MDIE-0001589 | Mindray Chemistry Analyzer [BS 230] | Class A |
| MDIE-0001967 | Mindray Endoscope Light Source [HB300 ] | Class A |
| MDIE-0001968 | Mindray Endoscope Light Source [HB500] | Class A |
| MDIE-0001969 | Mindray Endoscope Light Source [HB500R] | Class A |
| MDIR-0005382 | MINDRAY (Non -rechargeable public automated external defibrillator) | Class C |
| MDIR-0005383 | MINDRAY (Ventilator) [SV 600-SV 650-SV-800-SV-850] | Class C |
| MDIR-0005384 | MINDRAY (VENTILATOR: SV 70) | Class C |
| MDIR-0005385 | MINDRAY (HIV Ag/Ab Negative Control) | Class D |
| MDIR-0005386 | MINDRAY (HIV Ag/Ab Positive Control) | Class D |
| MDIR-0005387 | MINDRAY (Anti TP Calibrators) | Class C |
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.