High Flux Hemodialyzer, Hollow Fiber Hemodialyzer
Class B (low to moderate risk) · MDIR-0000945 · Progressive Corporation
DRAP REGISTERED MEDICAL DEVICE
High Flux Hemodialyzer, Hollow Fiber Hemodialyzer is registered with DRAP under number MDIR-0000945 as a Class B (low to moderate risk) medical device, imported. The listed holder is Progressive Corporation. Its listed renewal date (27 Nov 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000945 · 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 | High Flux Hemodialyzer, Hollow Fiber Hemodialyzer |
|---|---|
| Class | B |
| Listed holder | Progressive Corporation |
| Holder address | 147 -D, Commercial Broadway, Phase- 8 DHA, Lahore, Godown: Same as above |
| Manufacturing site | M/s. Suzhou Junkang Medical Technology Co., Ltd No.28 Wutaishan Road, SND 215163, Suzhou, Jiangsu, China |
| Issued | 28 Nov 2019 |
| Renewal date | 27 Nov 2024 |
| Licence | ELI-00114 |
Specifications
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Screened 7 Oct 2026, 07:52 (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-0001271 | SMARTFLUX LFP. 140 PUERMA M03534 | Class C |
| 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 |
Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
| MDIR-0006464 | Purifer (High Flux-Polyethersulfone Hollow Fiber Hemodialyzer) | Class C | MOODY Global Services |
| MDIR-0000709 | POLYPURE DIALYZER (10-22) (HOLLOW FIBER DIALYZER) Low Flux, Medim Flux, High Flux | Class C | Uniplan Trade International Pvt ltd |
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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.