DRAP REGISTERED MEDICAL DEVICE
DIAMAX WOW Single Patient Dialysis Machine is registered with DRAP under number MDIR-0004332 as a Class C (moderate to high risk) medical device, imported. The listed holder is Nipro Medical (Pvt) Ltd. It is listed as valid until 19 Dec 2027.
Screening result
MDIR-0004332 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00530
| Device | DIAMAX WOW Single Patient Dialysis Machine |
|---|---|
| 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 |
| Issued | 20 Dec 2022 |
| Renewal date | 19 Dec 2027 |
| Licence | ELI-00530 |
Specifications
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Screened 5 Oct 2026, 17:07 (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-0002656 | Nipro Sureflux Hemodialyzer [Sureflux E, Sureflux G, Sureflux L, Sureflux N] | Class C |
| MDIR-0002890 | Shunmei Hemodialysis Catheter Kit (Double lumen) | Class B |
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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.