DRAP REGISTERED MEDICAL DEVICE
SMARTFLUX LFP. 140 PUERMA M03534 is registered with DRAP under number MDIR-0001271 as a Class C (moderate to high risk) medical device, imported. The listed holder is Progressive Corporation. Its listed renewal date (11 Feb 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001271 · 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-00114
| Device | SMARTFLUX LFP. 140 PUERMA M03534 |
|---|---|
| Class | C |
| Listed holder | Progressive Corporation |
| Holder address | 147 -D, Commercial Broadway, Phase- 8 DHA, Lahore, Godown: Same as above |
| Manufacturing site | M/s. Medica S.p.A Via Degli Artigiani, 7 41036, Medolla (MO), Italy |
| Issued | 12 Feb 2020 |
| Renewal date | 11 Feb 2025 |
| Licence | ELI-00114 |
Specifications
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Screened 5 Oct 2026, 17:56 (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.
| MDIR-0000945 | High Flux Hemodialyzer, Hollow Fiber Hemodialyzer | Class B |
| MDIR-0002536 | Farco Fistula Fistula Needle (with Fixed Wing) Code: FSN1620, FSN1720, FSN1520 | Class B |
| MDIR-0002621 | FARCOLINE Sterile Blood Line [FBL00FR, FBL00GM] | Class B |
| MDIR-0004912 | ZOEY Hollow Fiber Hemodialyzer | Class C |
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.