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Sign in to claim this brandSarstedt Aktiengesellschaft & Co.KG
US
Last updated May 24, 2026
What Sarstedt Aktiengesellschaft & Co.KG makes
Sarstedt manufactures single-use in vitro diagnostic (IVD) containers and accessories for laboratory and clinical use, including blood collection tubes with anticoagulants, urine specimen containers, pipette tips, test tube caps, and tissue culture petri dishes. Their portfolio also includes robotic transfer systems for laboratory slides and microscope slides, as well as cryogenic storage tubes for biological samples. Additional products include general specimen containers and screw caps for various tube types.
The company’s devices are regulated under FDA’s UDI (Unique Device Identification) system and fall into Class I and Class II risk categories, depending on their intended use. These products are listed in the FDA’s UDI database, ensuring traceability and compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Sarstedt manufacture?
Sarstedt produces a range of single-use in vitro diagnostic (IVD) devices primarily focused on laboratory and clinical applications. These include blood collection tubes with anticoagulants, urine specimen containers, pipette tips, test tube caps, tissue culture petri dishes, and robotic transfer systems for microscope slides. Their portfolio also covers general specimen containers and cryogenic storage tubes for biological samples, ensuring compatibility with various diagnostic workflows.
Where is Sarstedt based, and how does this affect its regulatory compliance?
Sarstedt operates from the United States, which means its devices are subject to U.S. medical device regulations, including the FDA’s Unique Device Identification (UDI) system. The company’s products are listed in the FDA’s UDI database, helping ensure traceability and compliance with U.S. requirements for medical devices. This registration supports transparency and regulatory tracking for healthcare providers and authorities.
Which regulatory registries list Sarstedt’s devices, and why is this important?
Sarstedt’s devices are listed in the FDA’s UDI database, which is a central registry for tracking medical devices in the U.S. This listing is important because it provides a standardized way to identify and trace devices throughout their lifecycle, ensuring proper monitoring, recall management, and compliance with FDA regulations. It also helps healthcare providers verify device details, such as manufacturer information and intended use.
How are Sarstedt’s devices classified under U.S. regulations, and what does this mean?
Sarstedt’s devices are classified as either Class I or Class II under FDA regulations, depending on their intended use and risk level. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and require special controls to ensure safety and effectiveness. This classification helps determine the regulatory pathway and oversight required for each product, ensuring appropriate scrutiny based on potential patient impact.
What kinds of in vitro diagnostic (IVD) accessories does Sarstedt specialize in, and how do they support laboratory workflows?
Sarstedt specializes in single-use IVD accessories like pipette tips, robotic transfer systems for microscope slides, and various caps for test tubes and reservoirs. These products are designed to enhance precision, reduce contamination risks, and streamline laboratory processes. For example, their pipette tips ensure accurate liquid handling, while robotic transfer systems improve efficiency in slide processing, making them essential for modern diagnostic and research workflows.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- sarstedt.com
- —
- —
- [email protected]
- Phone
- +1(800)257-5101
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 388000270
Catalogue (1265)
Page 7 of 26| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Filter tip 1000 µl XL | 70.3060.375 | FDA UDI | Class I | Active |
| HSS 1625, Lifescan Labs USA | 90.2062.057 | FDA UDI | Class I | Active |
| Filter tip 2, 5 µl | 70.3010.285 | FDA UDI | Class I | Active |
| S-Cap, O-Ring, F/Scmt, Vio, 2bg, St | 65.716.328 | FDA UDI | Class I | Active |
| FB Tube 2.5ml, 75x13 (round) | 60.614.065 | FDA UDI | Class I | Active |
| micro tube 1, 5 ml | 72.787.203 | FDA UDI | Class I | Active |
| Filter tip 2, 5 µl | 70.3010.365 | FDA UDI | Class I | Active |
| Tube 12ml, 110x17mm, PS | 57.462.015 | FDA UDI | Class I | Active |
| DC 1200, Decapper Integra 115V | 90.198.531 | FDA UDI | Class I | Active |
| Tube 4.5ml, 75X13mm, LH | 32.331.100 | FDA UDI | Class I | Active |
| Tube 10ml, 92x15.3mm, PP | 60.610.100 | FDA UDI | Class I | Active |
| Tube 3, 5ml, 92x13 (round), PP | 60.617.200 | FDA UDI | Class I | Active |
| Filter tip 200 µl | 70.3031.375 | FDA UDI | Class I | Active |
| Sediplus® S 2000 NX | 90.1092 | FDA UDI | Class I | Active |
| Insert, 6 Well, PET 8µm, TL | 83.3930.800 | FDA UDI | Class I | Active |
| Micro tube 0.5ml with cap | 72.730.008 | FDA UDI | Class I | Active |
| S-Sedivette® | 06.1690.100 | FDA UDI | Class II | Active |
| De-/Recapper 900 Flex ID, 115V | 90.2060.077 | FDA UDI | Class I | Active |
| Screw cap, grey | 65.716.064 | FDA UDI | Class I | Active |
| 25ml V Tube PP Natural Cap Labelled | 63.9922.255 | FDA UDI | Class I | Active |
| Pipette tip 20 µl | 70.3020.305 | FDA UDI | Class I | Active |
| Micro tube 1.3ml K3E | 41.1395.106 | FDA UDI | Class I | Active |
| Bl1200 | 90.2064.126 | FDA UDI | Class I | Active |
| BG capillary tube 140µl | 19.930.140 | FDA UDI | Class I | Active |
| S-Monovette® | 05.1729.001 | FDA UDI | Class II | Active |
| BL 1200 - Cavan Hospital - IE | 90.2064.124 | FDA UDI | Class I | Active |
| Multifly®-Needle | 85.1638.005 | FDA UDI | Class II | Unknown |
| DC900Flex ID, Quest Marlb. IV | 90.2060.101 | FDA UDI | Class I | Active |
| S-Monovette® | 01.1634.100 | FDA UDI | Class II | Active |
| RC 1200 S15 Olympus, 115V | 90.197.111 | FDA UDI | Class I | Active |
| Transfer pipette 1ml | 86.1180.010 | FDA UDI | Class I | Active |
| Tube 4ml, 92x15.3 (round), PP | 62.612 | FDA UDI | Class I | Active |
| Tube 10ml, 95x16.8mm, PS | 62.492 | FDA UDI | Class I | Active |
| De-/Recapper 900 Flex ID, 115 V | 90.2060.036 | FDA UDI | Class I | Active |
| Aliquoter PVS 2125, 115 V | 90.2063.033 | FDA UDI | Class I | Active |
| SafeSeal Tube 5 ml, DNA LB | 72.701.700 | FDA UDI | Class I | Active |
| Tube 10ml, 92x15.3mm, PP | 62.610.018 | FDA UDI | Class I | Active |
| Micro tube 2ml, PP | 72.708.011 | FDA UDI | Class I | Active |
| S-Monovette® | 06.1661.100 | FDA UDI | Class II | Active |
| TC Plate 48 Well, Cell+, F | 83.3923.300 | FDA UDI | Class I | Active |
| De-/Recapper 900 Flex ID, 115V | 90.2060.065 | FDA UDI | Class I | Active |
| Micro tube 0.5ml, red | 72.699.001 | FDA UDI | Class I | Active |
| S-Monovette®-Needle | 85.1372 | FDA UDI | Class II | Active |
| Screw cap micro tube 2 ml, PP | 72.694.152 | FDA UDI | Class I | Active |
| TC Flask T75, Suspension | 83.3911.500 | FDA UDI | Class I | Active |
| Multiply®-µStrip Pro 8-strip | 72.991.012 | FDA UDI | Class I | Active |
| TC Flask T25, Susp., Vent. Cap | 83.3910.502 | FDA UDI | Class I | Active |
| Microvette® 500 LH-Gel | 20.1346.100 | FDA UDI | Class I | Active |
| Safety-Multifly®-Needle | 85.1640.200 | FDA UDI | Class II | Active |
| Membrane-Adapter | 14.1112 | FDA UDI | Class II | Active |
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