DRAP REGISTERED MEDICAL DEVICE
KORA 250 SR Pacemaker TPM013C (Single chamber rate responsive pacemaker MRI conditional). [TPM013C] is registered with DRAP under number MDIR-0004376 as a Class D (high risk) medical device, imported. The listed holder is Interex Company. It is listed as valid until 22 Dec 2027.
Screening result
MDIR-0004376 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00249
| Device | KORA 250 SR Pacemaker TPM013C (Single chamber rate responsive pacemaker MRI conditional). [TPM013C] |
|---|---|
| Class | D |
| Listed holder | Interex Company |
| Holder address | House No 195, 2nd Floor, KMCHS, Near Hill Park, Karachi. |
| Manufacturing site | M/s MicroPort CRM S.r.l Via Crescentino s.n. 13040 Saluggia (VC) Italy |
| Issued | 23 Dec 2022 |
| Renewal date | 22 Dec 2027 |
| Licence | ELI-00249 |
Specifications
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Screened 6 Oct 2026, 14:54 (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-0004375 | KORA 250 DR Pacemaker TPM010C (Dual chamber rate responsive pacemaker MRI conditional) [TPM010] | Class D |
| MDIR-0005416 | FLEBOGRIF Set for Venous Insufficiency Treatment [FLE6F90, FLE6F60] | 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.
