DRAP REGISTERED MEDICAL DEVICE
HemoSphere (Hemosphere Advance Monitoring Platform) is registered with DRAP under number MDIR-0006591 as a Class C (moderate to high risk) medical device, imported. The listed holder is Varitron. It is listed as valid until 6 Jun 2029.
Screening result
i
Imported device, registered with DRAP as Class C (moderate to high risk)
MDIR-0006591 · the class is taken from DRAP's list for this number
MDIR-0006591 · the class is taken from DRAP's list for this number
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 6 Jun 2029
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Holder has a DRAP import licence on file
ELI-00510
ELI-00510
| Device | HemoSphere (Hemosphere Advance Monitoring Platform) |
|---|---|
| Class | C |
| Listed holder | Varitron |
| Holder address | First Floor 60-D, F.C.C. Zahoor Elahi Road, Gulberg-IV, Lahore |
| Manufacturing site | M/s Edwards Lifesciences LLC One Edwards Way, IRVINE CA USA |
| Issued | 7 Jun 2024 |
| Renewal date | 6 Jun 2029 |
| Licence | ELI-00510 |
Specifications
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Screened 5 Oct 2026, 21:59 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
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| MDIR-0004979 | Litho (Surgical Laser) [35W] | Class C |
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| MDIR-0005120 | LITHO EVO (Surgical Laser) | Class C |
| MDIR-0005151 | Anthem Knee System | Class D |
| MDIR-0005280 | Fast Fix 360 (Meniscal Repair System) [IMPLANTS: 72202467, 72202468, 72202469 INSTRUMENTS: 72202674, 72202675] | Class C |
| MDIR-0005598 | Fiber Dust (Surgical Laser) [PFMS00005] | Class C |
| MDIR-0006374 | Swan-Ganz Thermodilution Catheter | Class D |
| MDIR-0006592 | Biorci HA (Bio absorbable Screws) | Class D |
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.