DRAP REGISTERED MEDICAL DEVICE
MONALISA Filler (Sterile Absorbable Injectable dermal filler) is registered with DRAP under number MDIR-0004981 as a Class D (high risk) medical device, imported. The listed holder is Aesthetic Alliance. It is listed as valid until 27 Mar 2028.
Screening result
MDIR-0004981
DRAP registered Class B/C/D list, 28 Aug 2025
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | MONALISA Filler (Sterile Absorbable Injectable dermal filler) |
|---|---|
| Class | D |
| Listed holder | Aesthetic Alliance |
| Holder address | House No. 418, Col. Sher Khan Shaheed Road, F-11/3, Islamabad |
| Manufacturing site | M/s Genoss Co., Ltd., 1F, Gyeonggi R&DB Center 226, GSaBC, 105 Gwanggyo-ro, Yeongtong-gu, Suwon-si, Gyeonggi-do, 443-270, Korea |
| Issued | 28 Mar 2023 |
| Renewal date | 27 Mar 2028 |
Specifications
No supplier specifications yet.
Supplier of this device? Add specifications (free during launch)
Sign in or create a free account to add specifications.
Screened 5 Oct 2026, 01:40 (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.
| MDIR-0004980 | MONALISA Lidocaine Filler (Sterile Absorbable Injectable dermal filler) | Class D |
Corrections
Is something on this page wrong? Report a correction
Corrections are checked against the evidence before anything changes on this page.
Screen another number
Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.