DRAP REGISTERED MEDICAL DEVICE
Renaf (Hollow Fibre Hemodialysis Dialyzer) [1.4 sq.m., 1.6 sq.m., 1.8 sq.m., 2.0 sq.m.] is registered with DRAP under number MDIR-0002992 as a Class C (moderate to high risk) medical device, imported. The listed holder is Renacon Pharma Ltd.. It is listed as valid until 14 Nov 2026.
Screening result
MDIR-0002992 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | Renaf (Hollow Fibre Hemodialysis Dialyzer) [1.4 sq.m., 1.6 sq.m., 1.8 sq.m., 2.0 sq.m.] |
|---|---|
| Class | C |
| Listed holder | Renacon Pharma Ltd. |
| Holder address | House No,3 Street No 1, 18 Km, Ferozepur Road, Mujahid Colony Lahore |
| Manufacturing site | M/s. Jiangxi Sanxin Medtee Co., Ltd No.999 Fushan Road, Xiaolan Economic Development Zone, Nanchang, Jiangxi, 330200, P.R. China |
| Issued | 15 Nov 2021 |
| Renewal date | 14 Nov 2026 |
Specifications
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Screened 5 Oct 2026, 21:10 (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-0002993 | Rena-Line BTL (Blood Tubing Line for Hemodialysis) | Class C |
| MDIR-0002994 | Renav AV Fistula Needle (Fistula Needle for Hemodialysis) | Class C |
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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.