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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 1 of 26| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Microvette® 200 Z-Gel | 20.1291 | FDA UDI | Class I | Active |
| CryoPure Tube 1.0ml red | 72.377.002 | FDA UDI | Class I | Active |
| BloodGas Monovette®2ml Ventilat | 05.1147.148 | FDA UDI | Class II | Active |
| Sc Mtube, 2ml, Brown, Cbs, Gwb, Asm | 72.694.311 | FDA UDI | Class I | Active |
| Pipette tip 200 µl | 70.3030.305 | FDA UDI | Class I | Active |
| Srew cap, orange | 65.716.326 | FDA UDI | Class I | Active |
| Micro tube 2ml, PP | 72.693.052 | FDA UDI | Class I | Active |
| Micro tube 2ml, PP | 72.694.100 | FDA UDI | Class I | Active |
| Micro tube 2.0ml, red | 72.691.002 | FDA UDI | Class I | Active |
| Multifly®-Needle | 85.1638.005 | FDA UDI | Class II | Active |
| Push cap, neutral | 65.723 | FDA UDI | Class I | Active |
| Screw cap, red | 65.716.732 | FDA UDI | Class I | Active |
| S-Monovette® | 04.1932.001 | FDA UDI | Class II | Active |
| SafeSeal tube 1.5ml, brown | 72.706.001 | FDA UDI | Class I | Active |
| Microvette® 100 K3E | 20.1278.100 | FDA UDI | Class I | Active |
| UriSet 24 without acid | 77.578.010 | FDA UDI | Class I | Active |
| De-/Recapper 900 Flex ID, 115V | 90.2060.080 | FDA UDI | Class I | Active |
| Micro tube 2ml, yellow | 72.689.004 | FDA UDI | Class I | Active |
| S-Monovette® | 02.1065.001 | FDA UDI | Class II | Active |
| SafeSeal tube 1.5ml, blue | 72.706.006 | FDA UDI | Class I | Active |
| Tube 10ml 97x16PS+Cap | 60.9921.821 | FDA UDI | Class I | Active |
| Multifly®-Needle | 85.1638.035 | FDA UDI | Class II | Active |
| Micro tube 1.5ml, PP | 72.687.772 | FDA UDI | Class I | Active |
| CryoPure Tube 4.5ml white | 72.383 | FDA UDI | Class I | Active |
| De-/Recapper 900 Flex ID, 115 V | 90.2060.030 | FDA UDI | Class I | Active |
| RC 900 Flex ID-MedFusion, Quest-USA | 90.2060.094 | FDA UDI | Class I | Active |
| Pipette tip 1250 µl XL | 70.3060.305 | FDA UDI | Class I | Active |
| Screw cap | 65.728.003 | FDA UDI | Class I | Active |
| TC Flask T75, Cell+, Vented Cap | 83.3911.302 | FDA UDI | Class I | Active |
| DC 1200, Decapper AU5800, 115V | 90.198.528 | FDA UDI | Class I | Active |
| Urine container 3.0 l | 77.575.001 | FDA UDI | Class I | Active |
| Recapper RC1200 Olympus, 115V | 90.197.011 | FDA UDI | Class I | Active |
| Membrane screw cap | 65.3716 | FDA UDI | Class I | Active |
| Tube 15ml, 120x17mm, PS | 62.553.042 | FDA UDI | Class I | Active |
| Sc Mtube, 2ml, Gwb, Red Cap, St | 72.694.323 | FDA UDI | Class I | Active |
| DCRC 900 Flex ID - Flow Health | 90.2060.112 | FDA UDI | Class I | Active |
| Safety-Needle | 85.1372.200 | FDA UDI | Class II | Active |
| TC Flask T175, Cell+ | 83.3912.300 | FDA UDI | Class I | Active |
| Micro tube 1.5ml, PP | 72.692.052 | FDA UDI | Class I | Active |
| Tube 5ml, 92x15.3mm, PP | 60.611.011 | FDA UDI | Class I | Active |
| Dc/Rc 900 Flex Id, Quest | 90.2060.086 | FDA UDI | Class I | Active |
| S-Cap, O-Ring, F/Scmt, Brn, 2bg, St | 65.716.329 | FDA UDI | Class I | Active |
| Micro tube 1.3ml FH | 41.1394.105 | FDA UDI | Class I | Active |
| Micro tube 2ml, PP | 72.609.054 | FDA UDI | Class I | Active |
| Seraplas | 53.677 | FDA UDI | Class I | Active |
| 8, 5 ml Urine Monovette | 10.258.081 | FDA UDI | Class I | Active |
| Micro tube 1.5ml, PP | 72.696 | FDA UDI | Class I | Active |
| 96 PCR Plate Biosphere® Plus | 72.985 | FDA UDI | Class I | Active |
| Micro tube 2ml, PP | 72.685 | FDA UDI | Class I | Active |
| Filter tip 100 µl | 70.3030.275 | FDA UDI | Class I | Active |
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