DRAP REGISTERED MEDICAL DEVICE
ACTOAIND Flache New 2.5g Polyhexamethylene biguanide hydrochloride, 8.0g didecyldimethylammon ium chloride and auxiliary substances (05.2232.2 (2lt) 05.2232.5 (5lt) is registered with DRAP under number MDIR-0004372 as a Class B (low to moderate risk) medical device, imported. The listed holder is Mezan International. It is listed as valid until 21 Dec 2027.
Screening result
MDIR-0004372 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00096
| Device | ACTOAIND Flache New 2.5g Polyhexamethylene biguanide hydrochloride, 8.0g didecyldimethylammon ium chloride and auxiliary substances (05.2232.2 (2lt) 05.2232.5 (5lt) |
|---|---|
| Class | B |
| Listed holder | Mezan International |
| Holder address | 59 BR II, Opp. DCO House, Haji Meherban Road, Jhelum |
| Manufacturing site | M/s ACTO Pharma HIJYEN SANAYI TIC. A.S Akcaburgaz Mahallesi, 3038 SoK No 11, 34522 Esenyurt Istanbul Turkey |
| Issued | 22 Dec 2022 |
| Renewal date | 21 Dec 2027 |
| Licence | ELI-00096 |
Specifications
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Screened 5 Oct 2026, 15:55 (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.