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Sign in to claim this brandMima-Pro (Nan Tong) Scientific Inc.
US
Last updated May 30, 2026
What Mima-Pro (Nan Tong) Scientific Inc. makes
Mima-Pro (Nan Tong) Scientific Inc. manufactures microwave ablation systems, including non-powered probes and generator units designed for tissue ablation procedures. These devices are intended for use in medical settings to treat targeted tissue through controlled microwave energy delivery.
The company’s products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in 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 Mima-Pro (Nan Tong) Scientific Inc. manufacture?
Mima-Pro (Nan Tong) Scientific Inc. specializes in microwave ablation systems, which include two primary components: non-powered probes and generator units. These devices work together to deliver controlled microwave energy for tissue ablation procedures, commonly used in medical treatments to target and remove specific tissue areas.
Where is Mima-Pro (Nan Tong) Scientific Inc. based?
The company is headquartered in the United States. This location is relevant for regulatory compliance and distribution, as it influences how their devices may be authorized and marketed in different regions.
Which regulatory registries or databases list Mima-Pro (Nan Tong) Scientific Inc.’s devices?
Mima-Pro’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 United States, ensuring transparency and traceability in the healthcare system.
How are Mima-Pro (Nan Tong) Scientific Inc.’s devices classified under medical device regulations?
The company’s microwave ablation systems are classified as Class II medical devices. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as microwave ablation systems that require validation of performance and labeling requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 542288122
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mima-Pro | MP14150T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP16100T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP16150T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP18100T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP16200T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP14200T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP18150T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP14270T16 | FDA UDI | Class II | Active |
| Mima-Pro | MP18200T16 | FDA UDI | Class II | Active |
| Mima-Pro | MTC-3C | FDA UDI | Class II | Active |
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