DRAP REGISTERED MEDICAL DEVICE
RunWay TM Guide Catheter is registered with DRAP under number MDIR-0000095 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-0000095 · 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 | RunWay TM Guide Catheter |
|---|---|
| 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 AvailMed S.A De C.V. C. Industrial Lt. 001 Mz. 105 No. 20905 Int. A, Col. Cd. Industrial Tijuana, Baja California 22444, Mexico |
| Issued | 6 Mar 2019 |
| Renewal date | 5 Mar 2024 |
| Licence | ELI-00120 |
Specifications
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Screened 5 Oct 2026, 18:34 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
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| MDIE-0000880 | Extractor Pro XL Retrieval Balloon Catheter | Class A |
| MDIE-0002092 | Permanent Sled Ultrasound Imaging Accessory H749393160100 | Class A |
| MDIR-0000043 | Accustick TM II Introducer System | Class B |
| MDIR-0000044 | LeVeen TM Standard Needle Electrode System | Class C |
| MDIR-0000045 | Rubicon TM 35 Support Catheter | Class B |
| MDIR-0000046 | Sterling TM Over-The-Wire PTA Balloon Dilatation Catheter | Class B |
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.
