DRAP REGISTERED MEDICAL DEVICE
Hubi cardiac duo (Tnl/CK-MB) (Tnl, CK-MB Determination kinase-MB) [ACDC-8025] is registered with DRAP under number MDIR-0005332 as a Class C (moderate to high risk) medical device, imported. The listed holder is Global Clinical Cura (Pvt) Ltd.. It is listed as valid until 26 Jul 2028.
Screening result
MDIR-0005332 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00196
| Device | Hubi cardiac duo (Tnl/CK-MB) (Tnl, CK-MB Determination kinase-MB) [ACDC-8025] |
|---|---|
| Class | C |
| Listed holder | Global Clinical Cura (Pvt) Ltd. |
| Holder address | House No. 18, Mian Iqbal Road, Westridge I, Rawalpindi. |
| Manufacturing site | M/s Humasis Co., Ltd Rm 114, 502,504,604,604-1, B03-1, B03-2, 88 Jeonpa-ro, Dongan-gu, Anyang-si Gyeonggi-do, Republic of Korea |
| Issued | 27 Jul 2023 |
| Renewal date | 26 Jul 2028 |
| Licence | ELI-00196 |
Specifications
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Screened 6 Oct 2026, 03:40 (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-0000844 | AVE Fully Automated Integrated Urine Analyzer [AVE-772] | Class A |
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| MDIE-0000896 | Vacutest Plast (K2ETDA 5.4mg) Reference no: 13510 (Lavender cap) | Class A |
| MDIE-0000897 | Vacutest Plast (Gel & K2ETDA) Reference no: 12620 (White cap) | Class A |
| MDIE-0000898 | Vacutest Plast (NaF and K2Ox) Reference no: 13806 (grey cap) | Class A |
| MDIE-0000899 | Vacutest Plast (Clot activator) Reference no: 11010 (red cap) | Class A |
| MDIE-0000900 | Vacutest Plast (Gel &Clot activator) Reference no: 10174, 10176 (Gold cap) | Class A |
| MDIE-0000901 | Vacutest Plast (Li & heparin 68 I.U) Reference no: 12010 (Green cap) | Class A |
| MDIR-0003930 | AccuVein (Vein Illumination System) [Av500] | Class B |
| MDIR-0005330 | HUBI Troponin 1 Troponin 1 Test | Class C |
| MDIR-0005331 | HUBI-Cardiac 3-in-1 Tn-I,CK-MC,Myoglobin Test | Class C |
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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.