Euro Flow
Class B (low to moderate risk) · MDIR-0007474 · K.M Enterprises
DRAP REGISTERED MEDICAL DEVICE
Euro Flow (IV Cannula) is registered with DRAP under number MDIR-0007474 as a Class B (low to moderate risk) medical device, imported. The listed holder is K.M Enterprises. It is listed as valid until 3 Nov 2029.
Screening result
MDIR-0007474 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00054
| Device | Euro Flow (IV Cannula) |
|---|---|
| Class | B |
| Listed holder | K.M Enterprises |
| Holder address | 605, D Block, M.A Johar Town, Lahore |
| Manufacturing site | M/s EuroMed for Medical Industries Area No.(10),Block(i) Free Zone,Nasr City, Cairo, Egypt |
| Issued | 4 Nov 2024 |
| Renewal date | 3 Nov 2029 |
| Licence | ELI-00054 |
Specifications
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Screened 7 Oct 2026, 06:09 (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.
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| MDIR-0001773 | Euro Flow I.V Cannula | Class B |
| MDIR-0001774 | Euro Flow Silicone Folly | Class B |
| MDIR-0002288 | AMD Disposable Infusion set with needle (Infusion Set) | Class B |
| MDIR-0002289 | AMD Disposable Syringes (Syringes for single use) [1ml, 10ml, 20ml] | Class B |
Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
| MDIR-0007395 | FRED X, Flow Re-Direction Endoluminal Device. Intracranial Neuro Vascular Stent | Class D | Intek Corporation |
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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.
