DRAP REGISTERED MEDICAL DEVICE
Restylane Lidocaine is registered with DRAP under number MDIR-0000226 as a Class D (high risk) medical device, imported. The listed holder is Noesis Pvt. Limited. Its listed renewal date (3 Mar 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000226 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00048
| Device | Restylane Lidocaine |
|---|---|
| Class | D |
| Listed holder | Noesis Pvt. Limited |
| Holder address | SCB Main, I.I Chundrigar Road, Karachi, Godown Address: Same as above |
| Manufacturing site | M/s Q-Med AB Seminariegatan 21, SE-752 28 Uppsala, Sweden |
| Issued | 4 Mar 2019 |
| Renewal date | 3 Mar 2024 |
| Licence | ELI-00048 |
Specifications
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Screened 6 Oct 2026, 11:28 (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.
| MDIR-0000227 | Restylane Skinboosters Vital Lidocaine | Class D |
| MDIR-0000228 | Restylane Lyft Lidocaine | 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.