DRAP REGISTERED MEDICAL DEVICE
Dialife(Hemodialyzers) is registered with DRAP under number MDIR-0005021 as a Class C (moderate to high risk) medical device, imported. The listed holder is Pharma Supply Corporation. It is listed as valid until 16 Apr 2028.
Screening result
i
Number type: imported, registered (Class B, C or D)
MDIR-0005021
MDIR-0005021
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 16 Apr 2028
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Holder has a DRAP import licence on file
ELI-00092
ELI-00092
| Device | Dialife(Hemodialyzers) |
|---|---|
| Class | C |
| Listed holder | Pharma Supply Corporation |
| Holder address | 49 J, Block-6, PECHS Nursery Karachi |
| Manufacturing site | M/s DIALIFE SA Industrial Center Vedeggio 3, Via al Fiume 3, 6807, Taverne, Switzerland |
| Issued | 17 Apr 2023 |
| Renewal date | 16 Apr 2028 |
| Licence | ELI-00092 |
Specifications
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Screened 4 Oct 2026, 23:52 (Pakistan time). A screening aid, not an official DRAP verification.
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| MDIR-0004755 | Kinmed I.V Cannula Safety-Y Type(Type IV) [III type (14G, 16G, 17G, 18G, 20G, 22G, 24G)] | Class B |
| MDIR-0004756 | Kinmed I.V Cannula with Wing (Type II) | Class B |
| MDIR-0004757 | Kinmed I.V Cannula with Injection Port (Type III) | Class B |
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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.