Medi Safe
Class B (low to moderate risk) · MDIR-0009281 · Al Fajar Traders
DRAP REGISTERED MEDICAL DEVICE
Medi Safe (Guide Wire) [PTFE] is registered with DRAP under number MDIR-0009281 as a Class B (low to moderate risk) medical device, imported. The listed holder is Al Fajar Traders. It is listed as valid until 6 May 2030.
Screening result
MDIR-0009281 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | Medi Safe (Guide Wire) [PTFE] |
|---|---|
| Class | B |
| Listed holder | Al Fajar Traders |
| Holder address | 133, J Block, Sabazazar, Lahore |
| Manufacturing site | M/s Tianck Medical Co Ltd 1-2 Floor, Building C,No.16 Yinkui road, Kuichong town, Dapeng new district, Shenzhen, 518119 Guangdong P.R. China |
| Issued | 7 May 2025 |
| Renewal date | 6 May 2030 |
Specifications
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Screened 7 Oct 2026, 04:53 (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.
| MDIE-0001294 | MediSafe Remover for skin stapler | Class A |
| MDIR-0008082 | MEDI SAFE Disposable Skin Staplers | Class B |
| MDIR-0009282 | MEDI SAFE Hemodialysis catheter [Straight Extension Tube Double Lumen] | Class B |
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Same device type listed by other holders, useful when comparing suppliers.
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| MDIR-0005317 | Medicare Safety Lancet | Class B | Mana & Co. |
| MDIE-0000694 | SAFE+ Mediplast (Saniplast) | Class A | A One Traders |
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.