DRAP REGISTERED MEDICAL DEVICE
EasyLyte Plus Na/K/Cl Analyzer is registered with DRAP under number MDIR-0002085 as a Class B (low to moderate risk) medical device, imported. The listed holder is Meditec Instruments Co.. Its listed renewal date (28 Jan 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002085 · 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-00233
| Device | EasyLyte Plus Na/K/Cl Analyzer |
|---|---|
| Class | B |
| Listed holder | Meditec Instruments Co. |
| Holder address | Suit No 202, Tahir Plaza, A-20, KCHSU, Near Duty Free Shop, Karachi., Godown Address: Same as Above |
| Manufacturing site | M/s Medica Corp., 5 Oak Park Drive, Bedford, MA 01730 USA |
| Issued | 29 Jan 2021 |
| Renewal date | 28 Jan 2026 |
| Licence | ELI-00233 |
Specifications
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Screened 6 Oct 2026, 02:44 (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-0002081 | EasyLyte Electrolyte Reagents [Cluster] | Class B |
| MDIR-0002082 | EasyRA Analyzer-ISE; LIS | Class B |
| MDIR-0002083 | EasyElectrolyte Analyzer Na/K/Cl | Class B |
| MDIR-0002084 | EasyBlood Gas Analyzer | Class B |
| MDIR-0002086 | EasyStat Analyzer | Class B |
| MDIR-0002087 | EasyLyte Electrodes [Cluster] | Class B |
| MDIR-0002413 | Finecare SARS CoV-2 IgG/IgM Test (Device) [Codes: W278] | Class C |
| MDIR-0002414 | EasyBloodGas Reagent Module and Quality Control (Cluster) | Class B |
| MDIR-0002518 | EasyRa Cholesterol Reagent Kit, CHOL | Class B |
| MDIR-0002519 | Finecare B-hCG Rapid Quantitative Test (Kit) Code: W225 | Class B |
| MDIR-0002520 | Finecare Vitamin D Rapid Quantitative Test (Kit) Code: W241 | Class B |
| MDIR-0002521 | Finecare D-Dimer Rapid Quantitative test (Kit) Code: W211 | Class C |
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.
