DRAP REGISTERED MEDICAL DEVICE
Lokum Amplatz Guide Wire is registered with DRAP under number MDIR-0001182 as a Class D (high risk) medical device, imported. The listed holder is SES Associates. Its listed renewal date (6 Jan 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001182 · 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-00041
| Device | Lokum Amplatz Guide Wire |
|---|---|
| Class | D |
| Listed holder | SES Associates |
| Holder address | 148-Ejaz Park, Model Town Link Road, Lahore |
| Manufacturing site | M/s. AndraTec GmbH Simmerner Str. 70, D-56075 Koblenz, Germany |
| Issued | 7 Jan 2020 |
| Renewal date | 6 Jan 2025 |
| Licence | ELI-00041 |
Specifications
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Screened 5 Oct 2026, 19:21 (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-0000251 | Nit-Occlud PFO: Double Umbrella System for Interventional Closure of PFO [Patent Foramen Ovale] | Class D |
| MDIR-0000252 | Nit-Occlud Le VSD | Class D |
| MDIR-0000253 | Nit-Occlud PDA Spiral System For Interventional Closure of PDA [Patent Ductus Arteriosus] | Class D |
| MDIR-0000254 | Nit-Occlud PDA-R | Class D |
| MDIR-0000255 | Nit-Occlud ASD-R | Class D |
| MDIR-0000256 | Multi Snare | Class B |
| MDIR-0000257 | Angiographic Catheter | Class D |
| MDIR-0000258 | Nit-Occlud Implantation Sheath [600080, 700080 ] | Class B |
| MDIR-0001181 | AltoSa-XL Gemini Balloon Catheter | Class D |
| MDIR-0001183 | Exeter Retrieval Snare Preloaded | Class D |
| MDIR-0001184 | AltoSa-XL PTA Balloon Catheter | Class D |
| MDIR-0002199 | MAGMA Rapamycin-Eluting Coronary Stent System | 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.
