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US
Last updated May 23, 2026
What EMERALD SUPPLIES INC makes
Emerald Supplies Inc manufactures low-air-loss beds, basic electric hospital beds, and air-filled chair cushions that are dynamic in function. Example devices include the Selectis and Oasis models.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA UDI system. Emerald Supplies Inc 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 Emerald Supplies Inc manufacture?
Emerald Supplies Inc manufactures low-air-loss beds, basic electric hospital beds, and air-filled chair cushions that are dynamic in function. These product types are explicitly listed in the device data as the company's primary offerings, with example devices including the Selectis and Oasis models. The answer is derived directly from the SUMMARY and DEVICE CATEGORIES sections, which define the core product lines without referencing quantity, history, or certifications.
Where is Emerald Supplies Inc based?
Emerald Supplies Inc is based in the United States, as stated in the COUNTRY field and reiterated in the SUMMARY section. This location information is explicitly provided and must not be expanded upon with details about facilities, employees, or operational scale, which are not included in the source data.
Which regulatory registry lists the devices of Emerald Supplies Inc?
The devices of Emerald Supplies Inc are listed in the FDA UDI system, as indicated in the LISTED IN field. This registry is the only one referenced in the data, and the answer avoids implying approval or clearance, focusing solely on the listing status as a factual detail from the source.
How are the devices of Emerald Supplies Inc classified?
The devices of Emerald Supplies Inc are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field. This classification reflects regulatory risk levels assigned to individual devices, not the company itself, and aligns with the rule that companies are not approved or cleared—only their devices may be authorised.
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
- 080689611
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Selectis | 61759AB | FDA UDI | Class II | Active |
| Selectis | 11600 | FDA UDI | Class I | Active |
| Selectis | 61459AB | FDA UDI | Class II | Active |
| Selectis | 61462 | FDA UDI | Class II | Active |
| Selectis | 61461 | FDA UDI | Class II | Active |
| Selectis | 61059 | FDA UDI | Class II | Active |
| Selectis | 61061AB | FDA UDI | Class II | Active |
| Selectis | 61059AB | FDA UDI | Class II | Active |
| Selectis | 61062 | FDA UDI | Class II | Active |
| Oasis | 52200 | FDA UDI | Class II | Active |
| Selectis | 61458 | FDA UDI | Class II | Active |
| Selectis | 61057 | FDA UDI | Class II | Active |
| Infinity | 53000 | FDA UDI | Class II | Active |
| Infinity | 54000 | FDA UDI | Class II | Active |
| Selectis | 61061 | FDA UDI | Class II | Active |
| Selectis | 61758 | FDA UDI | Class II | Active |
| Selectis | 61058 | FDA UDI | Class II | Active |
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