Medical device registration holder
Uniplan Trade International Pvt ltd
14 DRAP registrations and enlistments (4 Class B, 10 Class C) · Screen a DRAP number · Device types · Companies
DRAP lists
All devices of Uniplan Trade International Pvt ltd
| DRAP no. | Device | Class | Status |
|---|---|---|---|
| MDIR-0007404 | AmiCORE Apheresis kit-single needle with two platelet connectors and PAS connector (X7R8884) Apheresis Kit… | C | Valid to Nov 2029 |
| MDIR-0007403 | Amicus Apheresis Kitdouble needle with platelet addictive solution connector X7R2302 Apheresis Kits [X7R2302] | C | Valid to Nov 2029 |
| MDIR-0007402 | Amicus MNC apheresis kit double needle X7R2326 Apheresis Kits [X7R2326] | C | Valid to Nov 2029 |
| MDIR-0007401 | Amicus TPE plasma exchange kit X7R2349 Apheresis Kits [X7R2349] | C | Valid to Nov 2029 |
| MDIR-0005827 | DialMED (Hollow Fiber Hemodialyzer) | C | Valid to Dec 2028 |
| MDIR-0004735 | OCI Hollow Fiber Hemodialyzer (Polyethersulfone Hollow Fiber Hemodialyzer) | C | Valid to Feb 2028 |
| MDIR-0000709 | POLYPURE DIALYZER (10-22) (HOLLOW FIBER DIALYZER) Low Flux, Medim Flux, High Flux | C | Renewal passed |
| MDIR-0005624 | Topline (HDF) (Hollow Fiber Hemodialysis Dialyzer for Single Use) | C | Valid to Oct 2028 |
| MDIR-0009135 | UNILAS Touch One (CO2 Laser) [(30W) C20.00.000030, (40W), C20.00.000040] | C | Valid to Apr 2030 |
| MDIR-0009136 | UNILAS Touch Pro (CO2 Laser) [(60W) C20.00.000060, (70W) C20.00.000070, (80W) C20.00.000080] | C | Valid to Apr 2030 |
| MDIR-0003272 | AV Fistula Needle Sets (Fistula Needles) [V0801000103002 (E09541) V0801053103001 (E09641A) V0801103103001 (E09741A)] | B | Valid to Feb 2027 |
| MDIR-0003271 | Hemodialysis Blood Tubing Sets (Blood Tubing Line) [E07023, E07023-TP, E07507] | B | Valid to Feb 2027 |
| MDIR-0005626 | Topline (AVF) (A.V. Fistula Needle Set | B | Valid to Oct 2028 |
| MDIR-0005625 | Topline (BTL) (Sterile Hemodialysis Blood Circuits, for single use) | B | Valid to Oct 2028 |
Source: DRAP's published provisional lists of registered and enlisted medical devices. A screening aid, not an official DRAP verification.