Sarstedt AG & Co. KG
NUMBRECHT North Rhine-Westphalia, DE
SARSTEDT AG & CO. KG appears in FDA device records in NUMBRECHT North Rhine-Westphalia, DE. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 1 510(k) clearance for Sarstedt AG & Co. KG in 2023.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2023 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 9617475 | 3002808075 | SARSTEDT AG & CO. KG | Sarstedtstrasse 1, NUMBRECHT North Rhine-Westphalia 51588 DE | 2026 | and 13 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KXGApplicator, Absorbent Tipped, Sterile
- PJEBlood/Plasma Collection Device For Dna Testing
- JQCCentrifuges (Micro, Ultra, Refrigerated) For Clinical Use
- NNKContainer, Specimen Mailer And Storage, Non-Sterile
- KDTContainer, Specimen Mailer And Storage, Sterile
- NNLContainer, Specimen Mailer And Storage, Temperature Controlled, Non-Sterile
- JSMCulture Media, Non-Propagating Transport
- GKBDevice, Automated Sedimentation Rate
- KSDDevice, Heat-Sealing
- KZLDevice, Warming. Blood And Plasma
- KIZDish, Tissue Culture
- LXGEquipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- KJAFlask, Tissue Culture
- PPMGeneral Purpose Reagent
- JRCMicro Pipette
- GLEMixer, Blood Tube
- FPASet, Administration, Intravascular
- FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- JPHTest, Erythrocyte Sedimentation Rate
- GAXTourniquet, Nonpneumatic
- GIOTube, Collection, Capillary Blood
- GHCTube, Sedimentation Rate
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain