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Sign in to claim this brandErmis MedTech GmbH
US
Last updated May 24, 2026
What Ermis MedTech GmbH makes
Ermis MedTech GmbH manufactures reusable device sterilization and disinfection containers designed for medical equipment processing. These containers are engineered to safely hold and sterilize reusable medical devices, ensuring compliance with infection control protocols in clinical settings.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 Ermis MedTech GmbH manufacture?
Ermis MedTech GmbH specializes in reusable device sterilization and disinfection containers. These containers are specifically designed to safely hold and process reusable medical equipment, helping healthcare facilities meet infection control standards during sterilization procedures.
Where is Ermis MedTech GmbH based?
The company operates from the United States. While the name includes 'GmbH,' a German limited liability company suffix, the business itself is established and functions within the US market.
Which regulatory registries list Ermis MedTech GmbH’s devices?
Ermis MedTech GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US, ensuring transparency and traceability in the healthcare supply chain.
How are Ermis MedTech GmbH’s devices classified under FDA regulations?
The company’s sterilization and disinfection containers fall under Class II medical device classification by the FDA. This classification applies to devices that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- ermis-medizintechnik.de
- —
- —
- [email protected]
- Phone
- +4974619648570
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 313118522
Catalogue (516)
Page 3 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ermis | ER105.200E | FDA UDI | Class II | Active |
| Ermis | ER800.000P | FDA UDI | Class II | Active |
| Ermis | ER820.040 | FDA UDI | Class II | Active |
| Ermis | ER305.150ER7 | FDA UDI | Class II | Active |
| Ermis | ER306.100ER2 | FDA UDI | Class II | Active |
| Ermis | ER105.150ER1 | FDA UDI | Class II | Active |
| Ermis | ES191.050 | FDA UDI | Class II | Active |
| Ermis | ER200.010E | FDA UDI | Class II | Active |
| Ermis | ER600.050US | FDA UDI | Class II | Active |
| Ermis | ER105.135E | FDA UDI | Class II | Active |
| Ermis | ER300.030ER | FDA UDI | Class II | Active |
| Ermis | ER206.135ER7 | FDA UDI | Class II | Active |
| Ermis | ER106.150ER7 | FDA UDI | Class II | Active |
| Ermis | ER405.100E | FDA UDI | Class II | Active |
| Ermis | ER305.200ER1 | FDA UDI | Class II | Active |
| Ermis | ER822.070 | FDA UDI | Class II | Active |
| Ermis | ER820.060 | FDA UDI | Class II | Active |
| Ermis | ES181.100 | FDA UDI | Class II | Active |
| Ermis | ER660.060 | FDA UDI | Class II | Active |
| Ermis | ER100.070ER | FDA UDI | Class II | Active |
| Ermis | ER300.060ER | FDA UDI | Class II | Active |
| Ermis | ER205.100ER6 | FDA UDI | Class II | Active |
| Ermis | ER110.200E | FDA UDI | Class II | Active |
| Ermis | ER306.200ER6 | FDA UDI | Class II | Active |
| Ermis | ER601.050R | FDA UDI | Class II | Active |
| Ermis | ER590.035 | FDA UDI | Class II | Active |
| Ermis | ER305.100E | FDA UDI | Class II | Active |
| Ermis | ER100.030ER | FDA UDI | Class II | Active |
| Ermis | ER203.040E | FDA UDI | Class II | Active |
| Ermis | ER106.100E | FDA UDI | Class II | Active |
| Ermis | ER200.010ER | FDA UDI | Class II | Active |
| Ermis | ER821.050 | FDA UDI | Class II | Active |
| Ermis | ER305.260E | FDA UDI | Class II | Active |
| Ermis | ES180.010 | FDA UDI | Class II | Active |
| Ermis | ER206.150ER3 | FDA UDI | Class II | Active |
| Ermis | ER106.150E | FDA UDI | Class II | Active |
| Ermis | ER200.030E | FDA UDI | Class II | Active |
| Ermis | ER300.050ER | FDA UDI | Class II | Active |
| Ermis | ER305.100ER4 | FDA UDI | Class II | Active |
| Ermis | ER100.020ER | FDA UDI | Class II | Active |
| Ermis | ER822.060 | FDA UDI | Class II | Active |
| Ermis | ER601.030R | FDA UDI | Class II | Active |
| Ermis | ER190.070 | FDA UDI | Class II | Active |
| Ermis | ER200.030ER | FDA UDI | Class II | Active |
| Ermis | ER206.100ER5 | FDA UDI | Class II | Active |
| Ermis | ER820.100 | FDA UDI | Class II | Active |
| Ermis | ER411.040E | FDA UDI | Class II | Active |
| Ermis | ER305.100ER3 | FDA UDI | Class II | Active |
| Ermis | ER311.260E | FDA UDI | Class II | Active |
| Ermis | ER203.020E | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Ermis MedTech TUTTLINGEN Baden-Wurttemberg · DE FEI 3005071827