DRAP REGISTERED MEDICAL DEVICE
CARPENTIEREDWARDS Perimount (Biological Heart Valve) 3300 TFX is registered with DRAP under number MDIR-0004944 as a Class D (high risk) medical device, imported. The listed holder is Cardiac Care. It is listed as valid until 14 Mar 2028.
Screening result
MDIR-0004944 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00070
| Device | CARPENTIEREDWARDS Perimount (Biological Heart Valve) 3300 TFX |
|---|---|
| Class | D |
| Listed holder | Cardiac Care |
| Holder address | 848-C Shadman -1, Lahore |
| Manufacturing site | M/s Edwards Life sciences, LLC One Edwards Way Irvine, CA 92614, USA M/s Edwards lifesciences, (Singapore) Pte. Ltd. 35 Changi, North Cresent-Singapore 499641, Singapore |
| Issued | 15 Mar 2023 |
| Renewal date | 14 Mar 2028 |
| Licence | ELI-00070 |
Specifications
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Screened 5 Oct 2026, 16:07 (Pakistan time). A screening aid, not an official DRAP verification.
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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.