DRAP REGISTERED MEDICAL DEVICE
Verrata PLUS Pressure Guide Wire [10185P, 10185JP] is registered with DRAP under number MDIR-0001708 as a Class D (high risk) medical device, imported. The listed holder is Digital Imaging Systems. Its listed renewal date (18 Aug 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001708
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-00094
| Device | Verrata PLUS Pressure Guide Wire [10185P, 10185JP] |
|---|---|
| Class | D |
| Listed holder | Digital Imaging Systems |
| Holder address | 121- Habitat Apartments, Shadman II, Ghaus-ul-Azam Road, Lahore, Godown: Same as above |
| Manufacturing site | M/s Volcano Corporation 2870 Kilgore Rd, Rancho, Cordova, CA 95670 M/s Volcano Corporation by Volcarica S.R.L Coyol Free Zone and Business Park Building B37, Coyol, Alajuela Costa Rica |
| Issued | 19 Aug 2020 |
| Renewal date | 18 Aug 2025 |
| Licence | ELI-00094 |
Specifications
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Screened 4 Oct 2026, 22:10 (Pakistan time). A screening aid, not an official DRAP verification.
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| MDIR-0000014 | RX Acculink Carotid Stent System | Class D |
| MDIR-0000015 | Omnilink Elite Peripheral Stent System | Class C |
| MDIR-0000016 | Hi-Torque Whisper Guide Wire with Hydrophilic Coating | Class D |
| MDIR-0000017 | Hi-Torque Balance Middle Weight Guide Wire | Class D |
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.