UAB PROFARMA · 89-08 · LITHUANIA
For UAB PROFARMA, import alert is 89-08; country is LITHUANIA; import alert name is "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"; product is PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT | PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT | PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT | PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT; product code is 83 Q - - JR Reagents, 2019-novel coronavirus nucleic acid | 83 Q - - KO Reagent, coronavirus serological | 83 Q - - KP Coronavirus antigen detection test system. | 83 Q - - LT COVID-19 multi-analyte respiratory panel nucleic acid devices; date published is 10/28/2020; address is V. A. Graiciuno 6 , Vilnius, Vilnius County LITHUANIA, verified against its source on 2026-09-30.
- Firm
- UAB PROFARMA verified
- Import alert
- 89-08
- Import alert name
- "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"
- Country
- LITHUANIA verified
- Address
- V. A. Graiciuno 6 , Vilnius, Vilnius County LITHUANIA verified
- Date published
- 10/28/2020 verified
- Product code
- 83 Q - - JR Reagents, 2019-novel coronavirus nucleic acid | 83 Q - - KO Reagent, coronavirus serological | 83 Q - - KP Coronavirus antigen detection test system. | 83 Q - - LT COVID-19 multi-analyte respiratory panel nucleic acid devices each item verified
- Product
- PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT | PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT | PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT | PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT each item verified
- FDA notes
- Class III device, requires 510(k), or de novo application | Class III device, requires 510(k), or de novo application | Class III device, requires 510(k), or de novo application | Class III device, requires 510(k), or de novo application each item verified
What the source says
UAB PROFARMA Date Published : 10/28/2020 V. A. Graiciuno 6 , Vilnius, Vilnius County LITHUANIA
— accessdata.fda.gov, retrieved 2026-09-15
Where each value comes from
The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.
Product code, Product and FDA notes
83 Q - - JR Reagents, 2019-novel coronavirus nucleic acid Date Published: 10/28/2020 Desc: PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT Notes: Class III device, requires 510(k), or de novo application 83 Q - - KO Reagent, coronavirus serological Date Published: 10/28/2020 Desc: PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT Notes: Class III device, requires 510(k), or de novo application 83 Q - - KP Coronavirus antigen detection test system. Date Published: 10/28/2020 Desc: PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT Notes: Class III device, requires 510(k), or de novo application 83 Q - - LT COVID-19 multi-analyte respiratory panel nucleic acid devices Date Published: 10/28/2020 Desc: PRORAPID KIT CORONAVIRUS DISEASE (SARS-COV-2) IGG/IGM RAPID TEST CASSETTE SINGLE USE KIT Notes: Class III device, requires 510(k), or de novo application
— all from accessdata.fda.gov, retrieved 2026-09-15
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_244.html