ADVIA Centaur CK-MB - DRAP MDIR-0004506 (Class C)

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

i
Imported device, registered with DRAP as Class C (moderate to high risk)
MDIR-0004506 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 5 Feb 2028
✓
Holder has a DRAP import licence on file
ELI-00037
DeviceADVIA 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)
ClassC
Listed holderHoora Pharma (Pvt) Ltd
Holder addressWH-01 20-A7-A8, Korangi Creek Industrial Park, Karachi.
Manufacturing siteHealthcare 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.
Issued6 Feb 2023
Renewal date5 Feb 2028
LicenceELI-00037

Specifications

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Screened 6 Oct 2026, 01:27 (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.