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Sign in to claim this brandR. E. Morrison Equipment Inc
US
Last updated May 24, 2026
What R. E. Morrison Equipment Inc makes
R. E. Morrison Equipment Inc manufactures dental suction systems and medical device air compressors, including the BaseVac line. These products are designed for use in dental and medical environments to manage fluids and provide compressed air for procedures.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identification (UDI) system. 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 R. E. Morrison Equipment Inc manufacture?
R. E. Morrison Equipment Inc specializes in dental suction systems and medical device air compressors. These devices are primarily used in dental and medical settings to handle fluids during procedures and supply compressed air for equipment operation. The company’s focus is on products like the BaseVac line, which serves these critical functions.
Where is R. E. Morrison Equipment Inc based?
The company is based in the United States. This location is relevant for understanding regulatory frameworks, as it influences which authorities oversee the devices and where compliance requirements may apply.
Which regulatory registries list devices manufactured by R. E. Morrison Equipment Inc?
Devices from R. E. Morrison Equipment Inc are listed in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify medical devices in the United States, ensuring transparency and traceability for healthcare providers and regulators.
How are the devices produced by R. E. Morrison Equipment Inc classified by regulatory authorities?
The company’s devices, including the BaseVac line, fall under the FDA’s Class I classification. This classification typically applies to devices posing minimal risk to patients and users, often involving general controls like good manufacturing practices and labeling requirements. Class I devices are generally considered the lowest risk in the FDA’s hierarchy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- remequip.com
- —
- —
- [email protected]
- Phone
- 9058286301
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 246606479
Catalogue (69)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BaseVac | 2SUR4.16-3 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.25-1 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.40-2-3P | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.25-2 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-1-L | FDA UDI | Class I | Active |
| BaseVac | 1HD4.40P | FDA UDI | Class I | Active |
| BaseVac | S0.75 - 115 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.40-1 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-2 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.25-2-3P | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-1-3P | FDA UDI | Class I | Active |
| BaseVac | 2M4.25-230 | FDA UDI | Class I | Active |
| BaseVac | 2HD4 | FDA UDI | Class I | Active |
| BaseVac | S1.5E - 120 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-2-3P | FDA UDI | Class I | Active |
| BaseVac | 3HD4 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.40-3 | FDA UDI | Class I | Active |
| BaseVac | S1.5 - 230 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.25-1-3P | FDA UDI | Class I | Active |
| BaseVac | 4HD4 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.16-1 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.40-3-3P | FDA UDI | Class I | Active |
| BaseVac | D1.5 - 230 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.16-2 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.40-2-L | FDA UDI | Class I | Active |
| BaseVac | 2M4.16-230 | FDA UDI | Class I | Active |
| BaseVac | 2HD4.40P | FDA UDI | Class I | Active |
| BaseVac | 1SUR4.25-1 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.25-3 | FDA UDI | Class I | Active |
| BaseVac | 1SUR4.16-1 | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-3-3P | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.25-3-3P | FDA UDI | Class I | Active |
| BaseVac | 1SUR4.25+-1 | FDA UDI | Class I | Active |
| BaseVac | D2.0 - 230 | FDA UDI | Class I | Active |
| BaseVac | BVM1 | FDA UDI | Class I | Active |
| BaseVac | 2HD4.25P | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.40-2 | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.25-1-3P | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-1 | FDA UDI | Class I | Active |
| BaseVac | 1HD4.40A | FDA UDI | Class I | Active |
| BaseVac | 2HD4.25A | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.40-2 | FDA UDI | Class I | Active |
| BaseVac | 3HD4.40P | FDA UDI | Class I | Active |
| BaseVac | 3SUR4.25-2 | FDA UDI | Class I | Active |
| BaseVac | SCU.75E - 120 | FDA UDI | Class I | Active |
| BaseVac | 1HD4.25P | FDA UDI | Class I | Active |
| BaseVac | 2SUR4.25-2 | FDA UDI | Class I | Active |
| BaseVac | 1M4.16-120 MVAC | FDA UDI | Class I | Active |
| BaseVac | 1SUR4.40-1 | FDA UDI | Class I | Active |
| BaseVac | 1SUR4.40-2 | FDA UDI | Class I | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- R.e. Morrison Equipment Inc Mississauga Ontario · CA FEI 3005843821