DRAP ENLISTED MEDICAL DEVICE
IMPROVACUTER Blood Collection Tube (EDTA-K) [EDTA-K2: 1ml-2ml-3ml-4ml-4.5m l-5ml-6ml-7ml-7.5ml-8 ml-9ml-10ml] is enlisted with DRAP under number MDIE-0000369 as a Class A (low risk) medical device, imported. The listed holder is Mian Scientific Corporation (Pvt) Ltd.. It is listed as valid until 21 Feb 2027.
Screening result
MDIE-0000369
DRAP enlisted Class A list, 28 Aug 2025
ELI-00442
| Device | IMPROVACUTER Blood Collection Tube (EDTA-K) [EDTA-K2: 1ml-2ml-3ml-4ml-4.5m l-5ml-6ml-7ml-7.5ml-8 ml-9ml-10ml] |
|---|---|
| Class | A |
| Listed holder | Mian Scientific Corporation (Pvt) Ltd. |
| Holder address | Office No. 534, Jinnah Colony Faisalabad |
| Manufacturing site | M/s Guangzhou Improve Medical Instruments Co., Ltd., 102 Kaiyuan Avenue, science city, Guangzhou Economic & Technological Development District, Guangzhou, Guangdong, China. |
| Issued | 22 Feb 2022 |
| Renewal date | 21 Feb 2027 |
| Licence | ELI-00442 |
Specifications
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Screened 5 Oct 2026, 09:56 (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-0000363 | IMPROVACUTER Blood Collection Tube (No-Additive) [1ml-2ml-3ml-4ml-4.5 ml+5ml-6ml-7ml-8ml-9 ml-9.5ml-10ml] | Class A |
| MDIE-0000364 | IMPROVACUTER Blood Collection Tube (ESR-Sodium Citrate) [ESR tube (4 NC0.109M/.129M) 1.6ml-1.8ml-2ml-3ml-4 ml-5ml] | Class A |
| MDIE-0000365 | IMPROVACUTER Blood collection Tube [Glucose/Oxalate) [Glucose Tube: 2ml-3ml-4ml-5ml-6ml-: 15) Glucose Tube: 2ml-3ml3.5ml-4ml-5ml -6ml:16) Glucose Tube: 2ml-3ml4ml-5ml-6ml:… | Class A |
| MDIE-0000366 | IMPROVACUTER Blood Collection Tube (Lithium Heparin) [Lithium Heparin Tube: 1ml-2ml-3ml-4ml-5ml6ml-7ml-8ml-9ml ,5ml, 10ml] | Class A |
| MDIE-0000367 | IMPROVACUTER Blood Collection Tube (Sodium Citrate) Citrate Tube (9 NC0.109M/0129M) [2ml-3ml-4ml-5ml-6ml; 9ml-10ml; 9] | Class A |
| MDIE-0000368 | IMPROVACUTER Blood Collection Tube (Pro-Coagulation or Clot Activator) [Clot Activator Tube: 2ml-3ml-3.5ml-4ml-4.5 ml-5ml-6ml-7ml-8ml-9 ml-9.5ml-10ml] | Class A |
| MDIE-0000716 | ERBA (H-560 Hematology Analyzer) [H-560 (INS00078)] | Class A |
| MDIE-0000717 | ERBA (H-360 Hematology Analyzer) [H-360 (INS00077)] | Class A |
| MDIE-0000800 | Getein Immunofluorescence Quantitative Analyzer [Model:1100] | Class A |
| MDIE-0000921 | ERBA Xl-200 Chemistry Analyzer | Class A |
| MDIE-0000922 | ERBA Chem-7 Chemistry Analyzer | Class A |
| MDIE-0000932 | KWS No Additive Tube | Class A |
Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
| MDIE-0001096 | IMPROVACUTER BLOOD COLLECTION TUBE Sodium & lithium Heparin (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001097 | IMPROVACUTER BLOOD COLLECTION TUBE No Additive (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001098 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Lithium Heparin (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001099 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Sodium Heparin (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001100 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & EDTA.K2 (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001101 | IMPROVACUTER BLOOD COLLECTION TUBE Gel & Clot Activator (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001102 | IMPROVACUTER BLOOD COLLECTION TUBE ESR (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001103 | IMPROVACUTER BLOOD COLLECTION TUBE EDTA.K3 (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001104 | IMPROVACUTER BLOOD COLLECTION TUBE EDTA.K2 (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
| MDIE-0001105 | IMPROVACUTER BLOOD COLLECTION TUBE Clot Activator (Evacuated Blood Collection Tube) | Class A | Hoora Pharma (Pvt) Ltd |
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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.