DRAP REGISTERED MEDICAL DEVICE
PT2 TM Guidewire is registered with DRAP under number MDIR-0000133 as a Class D (high risk) medical device, imported. The listed holder is Ferozsons Laboratories Limited. Its listed renewal date (5 Mar 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000133 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00120
| Device | PT2 TM Guidewire |
|---|---|
| Class | D |
| Listed holder | Ferozsons Laboratories Limited |
| Holder address | Godown: Amangarh, Nowshera-KPK, Pakistan |
| Manufacturing site | M/s Boston Scientific Corporation 300, Boston Scientific Way, Marlborough, MA 01752 USA M/s Boston Scientific Corporation 302 Parkway, Global park, La Aurora, Heredia, Costa Rica |
| Issued | 6 Mar 2019 |
| Renewal date | 5 Mar 2024 |
| Licence | ELI-00120 |
Specifications
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Screened 6 Oct 2026, 16:00 (Pakistan time). A screening aid, not an official DRAP verification.
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Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
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| MDIR-0007411 | ASAHI GLADIUS MG-14 PV Guidewire | Class C | Tek Enterprises |
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| MDIR-0007415 | ASAHI GAIA NEXT (PTA guidewire) | Class D | Tek Enterprises |
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.