DRAP REGISTERED MEDICAL DEVICE
ADVIA Centaur CK-MB (10326496) Advia Centaur CKMB (10309982) Advia Centaur CKMB Calibrator (10311570) Advia Centaur CKMB Calibrator (10311572) Advia Centaur CKMB Diluent (10309951) Advia Centaur CKMB Diluent (10311592) is registered with DRAP under number MDIR-0004506 as a Class C (moderate to high risk) medical device, imported. The listed holder is Hoora Pharma (Pvt) Ltd. It is listed as valid until 5 Feb 2028.
Screening result
MDIR-0004506 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00037
| Device | ADVIA Centaur CK-MB (10326496) Advia Centaur CKMB (10309982) Advia Centaur CKMB Calibrator (10311570) Advia Centaur CKMB Calibrator (10311572) Advia Centaur CKMB Diluent (10309951) Advia Centaur CKMB Diluent (10311592) |
|---|---|
| Class | C |
| Listed holder | Hoora Pharma (Pvt) Ltd |
| Holder address | WH-01 20-A7-A8, Korangi Creek Industrial Park, Karachi. |
| Manufacturing site | Healthcare Diagnostics Products GmbH Emil- von-Behring- Strasse 76, 35041 Marburg, Germany. M/s Siemens Healthcare Diagnostics Inc., 333 Coney street east Walpole, MA, 02032, USA. |
| Issued | 6 Feb 2023 |
| Renewal date | 5 Feb 2028 |
| Licence | ELI-00037 |
Specifications
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Screened 6 Oct 2026, 01:27 (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-0001096 | IMPROVACUTER BLOOD COLLECTION TUBE Sodium & lithium Heparin (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001097 | IMPROVACUTER BLOOD COLLECTION TUBE No Additive (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001098 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Lithium Heparin (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001099 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Sodium Heparin (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001100 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & EDTA.K2 (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001101 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Clot Activator (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001102 | IMPROVACUTER BLOOD COLLECTION TUBE ESR (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001103 | IMPROVACUTER BLOOD COLLECTION TUBE EDTA.K3 (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001104 | IMPROVACUTER BLOOD COLLECTION TUBE EDTA.K2 (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001105 | IMPROVACUTER BLOOD COLLECTION TUBE Clot Activator (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001106 | IMPROVACUTER BLOOD COLLECTION TUBE Citrate (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001107 | IMPROVACUTER BLOOD COLLECTION TUBE Fluoride/ oxalate (Evacuated Blood Collection Tube) [Glucose/Fluoride/Oxal ate Tube: | Class A |
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.
