DRAP REGISTERED MEDICAL DEVICE
Invenia Abus 2.0 [Size: System] is registered with DRAP under number MDIR-0004967 as a Class B (low to moderate risk) medical device, imported. The listed holder is Hoora Pharma (Pvt) Ltd. It is listed as valid until 27 Mar 2028.
Screening result
i
Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0004967 · the class is taken from DRAP's list for this number
MDIR-0004967 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 27 Mar 2028
✓
Holder has a DRAP import licence on file
ELI-00037
ELI-00037
| Device | Invenia Abus 2.0 [Size: System] |
|---|---|
| Class | B |
| Listed holder | Hoora Pharma (Pvt) Ltd |
| Holder address | WH-01 20-A7-A8, Korangi Creek Industrial Park, Karachi. |
| Manufacturing site | M/s GE Medical System Ultrasound and Primary Care Diagnostics, LLC. 9900 Innovation Drive Wauwatosa, WI 53226. USA M/s GE Medical System [China] Co, Ltd. No. 19, Changjiang Road, Wuxi National Hi-Tech Dev. Zone, 214028 Jiangsu, China M/s GE Parallel Design, Inc. 4313 E. Cotton Blvd, Ste 100 Phoenix, AZ 85040, USA |
| Issued | 28 Mar 2023 |
| Renewal date | 27 Mar 2028 |
| Licence | ELI-00037 |
Specifications
No supplier specifications yet.
Supplier of this device? Add specifications (free during launch)
Sign in or create a free account to add specifications.
Screened 5 Oct 2026, 22:14 (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-0001096 | IMPROVACUTER BLOOD COLLECTION TUBE Sodium & lithium Heparin (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001097 | IMPROVACUTER BLOOD COLLECTION TUBE No Additive (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001098 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Lithium Heparin (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001099 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Sodium Heparin (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001100 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & EDTA.K2 (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001101 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Clot Activator (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001102 | IMPROVACUTER BLOOD COLLECTION TUBE ESR (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001103 | IMPROVACUTER BLOOD COLLECTION TUBE EDTA.K3 (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001104 | IMPROVACUTER BLOOD COLLECTION TUBE EDTA.K2 (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001105 | IMPROVACUTER BLOOD COLLECTION TUBE Clot Activator (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001106 | IMPROVACUTER BLOOD COLLECTION TUBE Citrate (Evacuated Blood Collection Tube) | Class A |
| MDIE-0001107 | IMPROVACUTER BLOOD COLLECTION TUBE Fluoride/ oxalate (Evacuated Blood Collection Tube) [Glucose/Fluoride/Oxal ate Tube: | Class A |
Corrections
Is something on this page wrong? Report a correction
Corrections are checked against the evidence before anything changes on this page.
Screen another number
Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.