DRAP REGISTERED MEDICAL DEVICE
(Hyamira Body) (Cross Linked Hyaluronic Acid) is registered with DRAP under number MDIR-0005613 as a Class C (moderate to high risk) medical device, imported. The listed holder is Schazoo SPL Consumer Healthcare. It is listed as valid until 24 Oct 2028.
Screening result
MDIR-0005613
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00095
| Device | (Hyamira Body) (Cross Linked Hyaluronic Acid) |
|---|---|
| Class | C |
| Listed holder | Schazoo SPL Consumer Healthcare |
| Holder address | 71-B/C2, Gulberg-III, Lahore |
| Manufacturing site | M/s Nyuma Pharma S.R.L, Via SanCarlo, 56-28041 Arona (NO) Italy |
| Issued | 25 Oct 2023 |
| Renewal date | 24 Oct 2028 |
| Licence | ELI-00095 |
Specifications
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Screened 5 Oct 2026, 12:12 (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-0000283 | Sampling swab Kits ( Viral Transport Medium (VTM) [AR150, AR100, AR120, AR121, ARY150, PRY150, AR105, AR180] | Class A |
| MDIR-0000898 | Esoxx Hyaluronic acid, Chondroitin Sulphate) 20 stick packs of 10 ml | Class D |
| MDIR-0000899 | Hyamira Basic (Reticulated Hyaluronic Acid: 20mg/ml) | Class D |
| MDIR-0000900 | Hyamira Forte (Reticulated Hyaluronic Acid: 25mg/ml) | Class D |
| MDIR-0000901 | Hyamira Soft (Reticulated Hyaluronic Acid: 15mg/ml) | Class D |
| MDIR-0000902 | Hyamira (Cross-linked Hyaluronic Acid Sodium Salt in prefilled syringe) 1.6% - 16mg/1ml and 32mg/2ml 2.0% -… | Class D |
| MDIR-0001703 | Hyacorp Lips (Hylan Gel) | Class D |
| MDIR-0001704 | Hyacorp Face (Hylan Gel) | Class D |
| MDIR-0001705 | Hyacorp Body Contouring MLF2 (Hylan Gel Contour) | Class D |
| MDIR-0001706 | Hyacorp Fine (Hylan Solution) | Class D |
| MDIR-0001707 | Hyacorp Body Contouring MLF1 (Hylan Gel Contour) | Class D |
| MDIR-0002287 | Vijoint hcc60 mg/3ml. (Hyaluronic acid Sodium Salt, Chondroitin Sulfate, Cyclodextrin) | 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.