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| # | Company | Amount | Rank | Status |
|---|---|---|---|---|
| 1 | L1₹10.71Admitted-Finance PLOT NO 348 ALPINE BIOMEDICALS PVT LTD 348 SECTOR 2 IGC HSIIDC SAHA INDUSTRIAL AREA DISTT AMBALA HARYANA 133104 SAHA INDUSTRIAL AREA | AMBALA | HARYANA | 133104 | L1 | Admitted-Finance | |
| 2 | L2₹21.69+₹10.98 (102.5%)Admitted-Finance MUMBAI | L2 | Admitted-Finance | |
| 3 | Rejected-Technical 1209 12TH FLOOR D MALL PLOT NO A1 NETAJI SUBHASH PLACE PITAMPURA DELHI DELHI INDIA 110034 | DELHI | DELHI | DELHI | 110034 | - | Rejected-Technical NonResponsive as per order no 1879 Dt 21.10.2026 | |
| 4 | Rejected-Technical 396 L T FLAT 4TH FLOOR LIG FLAT SECTOR 18B DWARKA SOUTH WEST DELHI DELHI 110078 | SOUTH WEST DELHI | DELHI | 110078 | - | Rejected-Technical NonResponsive as per order no 1879 Dt 21.10.2026 | |
| 5 | Rejected-Technical | - | Rejected-Technical NonResponsive as per order no 1879 Dt 21.10.2026 |
| Sl No | Description | Qty | Unit | MERIL DIAGNOSTICS PVT. LTD L2 | Alpine Biomedicals Pvt Ltd L1 |
|---|---|---|---|---|---|
| 1.00 | "SyphilisAntibody (Rapid) detection kits
1. The assay should be based on Rapid chromatographic immunoassay for qualitative detection of Antibodies (lgG, lgA & lgM) to TP in serum, plasma & whole Blood.
2. The assay should utilize recombinant Treponemal antigens i.e. Tp15, Tpl7, Tp47 against Syphilis.
3. The assay should be in card format.
4. Adequate documents detailing the principle components, bio- safety methodologies, validity criteria, interpretation of results, performance characteristics storage conditions, limitation of assays manufacturing & expiry dates should be provides with each kit.
5. The kit should have approval of the statutory authority in its country of origin.
6. In case of imported kits it should be registered and licensed under the provisions of Drugs & Cosmetics act and rules and/or medical devices rules 2017 in India.
7. In case of indigenous manufacturers should be licensed under the provisions of Drugs & cosmetics Act and rules and or medical devices rules 2017 issued by the competent authority defined under Drugs and cosmetics act, 1940.
8. The kit should have minimum shelf- life of 5/6th or 12 months (whichever is more) at the port of discharge of consignees.
9. Read result time should not be more than 20 minutes.
10. Assay should have Sensitivity 100% & specificity 99 %or more with documentary evidence.
11. The storage & transport temperature of the Kit should be 2-30°C.
12. The pack size should not be more than 50 tests wherein each test is individually
" | 8,00,000 | pack size should not be more than 50 tests But rate should be coated each test | 13.5 ₹14.18 | 5.4 ₹5.67 Lowest |
| 2.00 | Bed Side Leucodepletion Filters for Blood Transfusion (For 2 unit of Red Cell) [NE32B] 1. Filters should be able to leucodeplete
red cells form leukocyte
contamination separately for 1 unit
of red cells and for 2 units of red
cells each.
2. Filters should be having the
capacity of log 4 reduction
(99.99%)
3. Filters should not carry any
charges it should be neutrally
charged.
4. Filters material should be
polyester woven / non- woven.
5. Leukocytes should be
consistently averaging less than
0.5x105 residual leucocytes for
one unit of red cell and 0.2*106
for two units of red cell. RBC
recovery should be averaging more
than 90%.
6. Filters should have hard / soft
housing for optical monitoring.
7. Filtration loss should not be
more than 35 ml for one unit red
cell.
8. Should have integrated ≥ 40 μm,
micro aggregate filter.
9. Should be US FDA/ European
CE Certified. | 16,500 | Filter should have individual packing with bulk box pack. Quantity should be in multi ple of 05 units box(Rate shoul d be quoted for Each Filter) | - | - |
| 3.00 | Hepatitis B Surface Antigen (Elisa) Testing Kits IV Generation/High sensitive
Should have Microplate ELISA Coated with either polyclonal or monoclonal antibodies to HBsAg and either polyclonal or monoclonal antibodies in conjugate. The assay should be able to detect all the 11 subtypes (ad & ay subtype) including mutant strains. The assay should be able to detect surface antigen to hepatitis B virus. | 12,21,331 | 96 test/kit (kit containing 96 test) Rate should be quoted for each test. | - | - |
| 4.00 | HBsAg (Rapid Test) | 13,54,052 | The pack size should not be more than 50 tests wherein each test is individually packed. (Rate should be quoted for each test) | 7.16 ₹7.52 | 4.8 ₹5.04 Lowest |
Tender Value
₹4.4 Cr
EMD Value
₹8.8 L
Closing Date
2 Jun 2026, 6:00 pmClosed
MD RMSC
RMSCL, Swasthya Bhawan , Tilak Marg, C-Scheme Jaipur
SHORT TERM E-BID FOR RATE CONTRACT CUM SUPPLY AND EMPANELMENT OF SURGICAL ITEMS
2026_RMSCL_555002_1
F02 219 RMSCL Proc S and S NIB 14 2026 1070 Dt. 29.04.2026
Open Tender
Supply of Materials/Hiring of Goods
Item Rate
75 days
All Rajasthan
As Per Bid Condition
4 documents required · 4 mandatory
₹2,360
Yes
MD RMSCL
₹8.8 L
Yes
RMSCL(BOARD ROOM)
22 Oct 2026
29 Apr 2026
3 Jun 2026
29 Apr 2026
2 Jun 2026
8 May 2026
6 May 2026
| Sl No | Description | Qty | Unit | Est. Rate | Est. Amount |
|---|---|---|---|---|---|
| 1 | "SyphilisAntibody (Rapid) detection kits
1. The assay should be based on Rapid chromatographic immunoassay for qualitative detection of Antibodies (lgG, lgA & lgM) to TP in serum, plasma & whole Blood.
2. The assay should utilize recombinant Treponemal antigens i.e. Tp15, Tpl7, Tp47 against Syphilis.
3. The assay should be in card format.
4. Adequate documents detailing the principle components, bio- safety methodologies, validity criteria, interpretation of results, performance characteristics storage conditions, limitation of assays manufacturing & expiry dates should be provides with each kit.
5. The kit should have approval of the statutory authority in its country of origin.
6. In case of imported kits it should be registered and licensed under the provisions of Drugs & Cosmetics act and rules and/or medical devices rules 2017 in India.
7. In case of indigenous manufacturers should be licensed under the provisions of Drugs & cosmetics Act and rules and or medical devices rules 2017 issued by the competent authority defined under Drugs and cosmetics act, 1940.
8. The kit should have minimum shelf- life of 5/6th or 12 months (whichever is more) at the port of discharge of consignees.
9. Read result time should not be more than 20 minutes.
10. Assay should have Sensitivity 100% & specificity 99 %or more with documentary evidence.
11. The storage & transport temperature of the Kit should be 2-30°C.
12. The pack size should not be more than 50 tests wherein each test is individually
" | 8,00,000 | pack size should not be more than 50 tests But rate should be coated each test | - | - |
| 2 | Bed Side Leucodepletion Filters for Blood Transfusion (For 2 unit of Red Cell) [NE32B] 1. Filters should be able to leucodeplete
red cells form leukocyte
contamination separately for 1 unit
of red cells and for 2 units of red
cells each.
2. Filters should be having the
capacity of log 4 reduction
(99.99%)
3. Filters should not carry any
charges it should be neutrally
charged.
4. Filters material should be
polyester woven / non- woven.
5. Leukocytes should be
consistently averaging less than
0.5x105 residual leucocytes for
one unit of red cell and 0.2*106
for two units of red cell. RBC
recovery should be averaging more
than 90%.
6. Filters should have hard / soft
housing for optical monitoring.
7. Filtration loss should not be
more than 35 ml for one unit red
cell.
8. Should have integrated ≥ 40 μm,
micro aggregate filter.
9. Should be US FDA/ European
CE Certified. | 16,500 | Filter should have individual packing with bulk box pack. Quantity should be in multi ple of 05 units box(Rate shoul d be quoted for Each Filter) | - | - |
| 3 | Hepatitis B Surface Antigen (Elisa) Testing Kits IV Generation/High sensitive
Should have Microplate ELISA Coated with either polyclonal or monoclonal antibodies to HBsAg and either polyclonal or monoclonal antibodies in conjugate. The assay should be able to detect all the 11 subtypes (ad & ay subtype) including mutant strains. The assay should be able to detect surface antigen to hepatitis B virus. | 12,21,331 | 96 test/kit (kit containing 96 test) Rate should be quoted for each test. | - | - |
| 4 | HBsAg (Rapid Test) | 13,54,052 | The pack size should not be more than 50 tests wherein each test is individually packed. (Rate should be quoted for each test) | - | - |
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