DRAP REGISTERED MEDICAL DEVICE
Nipro Sureflux Hemodialyzer [Sureflux E, Sureflux G, Sureflux L, Sureflux N] is registered with DRAP under number MDIR-0002656 as a Class C (moderate to high risk) medical device, imported. The listed holder is Nipro Medical (Pvt) Ltd. Its listed renewal date (18 Jul 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002656 · 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-00530
| Device | Nipro Sureflux Hemodialyzer [Sureflux E, Sureflux G, Sureflux L, Sureflux N] |
|---|---|
| Class | C |
| Listed holder | Nipro Medical (Pvt) Ltd |
| Holder address | Building No.24, Central Commercial Area, DHA Phase 8, Ex-Park View, Lahore |
| Manufacturing site | M/s Nipro Corporation 3-9-3, Honjo-Nishi, Kita-ku, Osaka 531-8510, Japan M/s Nipro Corporation Odate Factory 8-7, Hanukiyachi, Niida, Odate-shi, Akita, 018-5794 Japan |
| Issued | 19 Jul 2021 |
| Renewal date | 18 Jul 2026 |
| Licence | ELI-00530 |
Specifications
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Screened 6 Oct 2026, 08:05 (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-0001595 | Nipro Set Blood Tubing Set [A071 (I)(8mm)/V648(I), A071 (I)/V648(I)] | Class B |
| MDIR-0001596 | Nipro AV Fistula Needle [G14,G15, G16 &G17] | Class B |
| MDIR-0001597 | Nipro Elisio (Hemodialyzer) | Class C |
| MDIR-0002344 | Nipro RO Medical (Water Treatment System for Dialysis) | Class C |
| MDIR-0002345 | NiproCart A2F (Powder Sodium Bicarbonate Cartridge for Hemodialysis) | Class C |
| MDIR-0002346 | Nipro Elisio Hemodialyzer (Synthetic hemodialyzer) | Class C |
| MDIR-0002347 | Surdial X (Single patient Dialysis Machine) | Class C |
| MDIR-0002348 | Surdial 55 plus (Single Patient Dialysis Machine) | Class C |
| MDIR-0002366 | Nipro Extracorporeal Blood Circuit (Blood Tubing Set) | Class B |
| MDIR-0002412 | JMI Auto Disable Syringe [0.1ml, 0.5ml, 3ml, 5ml, 10ml] | Class B |
| MDIR-0002890 | Shunmei Hemodialysis Catheter Kit (Double lumen) | Class B |
| MDIR-0004332 | DIAMAX WOW Single Patient Dialysis Machine | 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.