DRAP REGISTERED MEDICAL DEVICE
Leforte System [Bone Plate and Bone Screw] is registered with DRAP under number MDIR-0003175 as a Class C (moderate to high risk) medical device, imported. The listed holder is TraMax Health Systems. It is listed as valid until 21 Feb 2027.
Screening result
MDIR-0003175 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00026
| Device | Leforte System [Bone Plate and Bone Screw] |
|---|---|
| Class | C |
| Listed holder | TraMax Health Systems |
| Holder address | A-337 Block -D, North Nazimabad, Karachi. |
| Manufacturing site | M/s Jeil Medical Corporation 702-703-704-705-706-805-807-812-ho, 55, Digital-ro-gil, Guro-gu, Seoul, Korea |
| Issued | 23 Feb 2022 |
| Renewal date | 21 Feb 2027 |
| Licence | ELI-00026 |
Specifications
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Screened 6 Oct 2026, 16:25 (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-0003174 | Leforte Neuro System [Bone Plate and Bone Screw] | 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.