Pe-Ha-Luron F 3.0%.
Class B (low to moderate risk) · MDIR-0002211 · Mubarik Vision
DRAP REGISTERED MEDICAL DEVICE
Pe-Ha-Luron F 3.0%. (Hymaluronic Acid (Ophth. Intraocular Devices) is registered with DRAP under number MDIR-0002211 as a Class B (low to moderate risk) medical device, imported. The listed holder is Mubarik Vision. Its listed renewal date (15 Feb 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002211 · 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.
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | Pe-Ha-Luron F 3.0%. (Hymaluronic Acid (Ophth. Intraocular Devices) |
|---|---|
| Class | B |
| Listed holder | Mubarik Vision |
| Holder address | Baserment 32-A Usman Center, Shah Alam Market, Lahore, Godown: Same as above |
| Manufacturing site | M/s Albomed GmbH Hildebrandstrasse 11 D-90592 Schwarzenbruck, Germany M/s Sothema BP1 Industrial Zone Bouskoura, Casablanca Morocco |
| Issued | 16 Feb 2021 |
| Renewal date | 15 Feb 2026 |
Specifications
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Screened 7 Oct 2026, 04:54 (Pakistan time). A screening aid, not an official DRAP verification.
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Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
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| MDIR-0009113 | Neauvia Intense Rheology Hyaluronic acid hydrogels Cross-linked 22mg/ml | Class D | Schazoo SPL Consumer Healthcare |
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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.
