Euro-Ject
Class B (low to moderate risk) · MDIR-0002290 · K.M Enterprises
DRAP REGISTERED MEDICAL DEVICE
Euro-Ject (Disposable Syringe) [1ml, 10ml] is registered with DRAP under number MDIR-0002290 as a Class B (low to moderate risk) medical device, imported. The listed holder is K.M Enterprises. Its listed renewal date (11 Mar 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002290 · 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.
ELI-00054
| Device | Euro-Ject (Disposable Syringe) [1ml, 10ml] |
|---|---|
| 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 | 12 Mar 2021 |
| Renewal date | 11 Mar 2026 |
| Licence | ELI-00054 |
Specifications
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Screened 7 Oct 2026, 02:03 (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.
| MDIE-0000130 | Maxpro (Latex Examination gloves) | Class A |
| MDIE-0000230 | AMD SURGICAL Disposable Face Mask | Class A |
| MDIE-0000231 | BIOMAX (Latex Examination Gloves) | Class A |
| MDIE-0000729 | AMD Disposable Urine Bag [2000ML] | Class A |
| MDIE-0000891 | HD Vacuum Blood Collection Tube | Class A |
| MDIR-0000597 | Carex Non-Medicated Natural Rubber Latex Male Condoms | Class D |
| MDIR-0001651 | EVES (IUCD Copper T 380A) | Class D |
| MDIR-0001772 | Euro Flow Foley Catheters | Class B |
| 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 |
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.
