Versa Trek Redox - DRAP MDIE-0000768 (Class A)

DRAP ENLISTED MEDICAL DEVICE

Versa Trek Redox (Blood Culture Media) is enlisted with DRAP under number MDIE-0000768 as a Class A (low risk) medical device, imported. The listed holder is Vantage Technologies. It is listed as valid until 17 Dec 2028.

Screening result

i
Imported device, enlisted with DRAP as Class A (low risk)
MDIE-0000768 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP enlisted Class A list, 28 Aug 2025
✓
Listed valid until 17 Dec 2028
✓
Holder has a DRAP import licence on file
ELI-00219
DeviceVersa Trek Redox (Blood Culture Media)
ClassA
Listed holderVantage Technologies
Holder address251, Street 11-B, Phase-1, Ghouri Town, Islamabad Highway, Islamabad
Manufacturing siteM/s Remel Inc. a subsidiary of Thermo Fisher Scientific USA, 12076 Santa Fe Trail Drive, Lenexa, Kansas, USA M/s Thermo Fisher Scientific LLC 275 Aiken Road Asheville, NC 288804 USA
Issued18 Dec 2023
Renewal date17 Dec 2028
LicenceELI-00219

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

Other DRAP registrations and enlistments listed for the same company.

MDIE-0000115Versa Trek Instrument 240 (Automated Blood Culture System) [6240-04, 6240-06, 6240-08, 6240-10]Class A
MDIE-0000668Versa Trek 528 Microbial Detection System [Automated Blood Culture System] [6528-22, 6528-22M]Class A
MDIE-0002049V-TUBE-EDTA Plastic Tube Blood Collection TubeClass A
MDIE-0002050V-TUBE-Serum Separator Gel Plastic Tube Clot Activator with Gel Blood Collection TubeClass A
MDIE-0002051V-TUBE Citrate Plastic Tube Citrate Blood Collection TubeClass A
MDIE-0002052V-TUBE-Serum Plastic Tube Clot Active Serum Blood Collection TubeClass A
MDIE-0002053V-TUBE-Heparin Plastic Tube Heparin Blood Collection TubeClass A
MDIE-0002054V-TUBE-Glucose Evacuated Plastic Tube Fluoride EDTA / Glucose Blood Collection TubeClass A

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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.