DRAP REGISTERED MEDICAL DEVICE
Perfectha Finelines Lidocaine [PDFLL (1x1ml) Accessories (2 x 30G x13mm needles Plunger rod and backstop)] is registered with DRAP under number MDIR-0003521 as a Class D (high risk) medical device, imported. The listed holder is Schazoo SPL Consumer Healthcare. It is listed as valid until 27 Jun 2027.
Screening result
MDIR-0003521
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00095
| Device | Perfectha Finelines Lidocaine [PDFLL (1x1ml) Accessories (2 x 30G x13mm needles Plunger rod and backstop)] |
|---|---|
| Class | D |
| Listed holder | Schazoo SPL Consumer Healthcare |
| Holder address | 71-B/C2, Gulberg-III, Lahore |
| Manufacturing site | M/s Sinclair France SAS 8 Chemin du Jubin, F-69570 Dardilly, France |
| Issued | 28 Jun 2022 |
| Renewal date | 27 Jun 2027 |
| Licence | ELI-00095 |
Specifications
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Screened 4 Oct 2026, 23:52 (Pakistan time). A screening aid, not an official DRAP verification.
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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.