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Sign in to claim this brandWhat Solomed, S.A. de C.V. makes
Solomed, S.A. de C.V. manufactures one-piece intestinal ostomy bags that are open-ended, exudate-absorbent dressings with hydrophilic gel and no antimicrobial properties, and single-use surgical gowns. The company also produces pressure bandages made from Hevea-latex that are single-use and non-sterile, thoracic suction collection containers, synthetic polymer semi-permeable film dressings that are adhesive, and medical device disinfection agents.
The devices in Solomed's portfolio are classified as Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) system. The company 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 Solomed, S.A. de C.V. manufacture?
Solomed, S.A. de C.V. manufactures one-piece intestinal ostomy bags that are open-ended, exudate-absorbent dressings with hydrophilic gel and no antimicrobial properties, single-use surgical gowns, pressure bandages made from Hevea-latex that are single-use and non-sterile, thoracic suction collection containers, synthetic polymer semi-permeable film dressings that are adhesive, and medical device disinfection agents. These product types are derived directly from the device categories and example devices listed in the provided data.
Where is Solomed, S.A. de C.V. based?
Solomed, S.A. de C.V. is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this location, indicating the company’s operational base within the U.S.
Which regulatory registry lists the devices made by Solomed, S.A. de C.V.?
The devices manufactured by Solomed, S.A. de C.V. are listed in the FDA's Unique Device Identification (fda_udi) system, as specified in the LISTED IN field and reiterated in the SUMMARY. This registry is used for tracking medical devices in the U.S. market.
How are the devices made by Solomed, S.A. de C.V. classified?
The devices in Solomed's portfolio are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field and confirmed in the SUMMARY. This classification reflects the risk level and regulatory controls applicable to each device type, with no implication of company-wide approval.
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
- 588625921
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Osto System | Adult | FDA UDI | Class I | Active |
| Osto System | Adult | FDA UDI | Class I | Active |
| Hidroderm | 15 x 16 cm | FDA UDI | Class I | Active |
| SOLOMED Disposable Surgical Gown | Medium Size | FDA UDI | Class I | Active |
| Hidroderm | 10 x 10 cm | FDA UDI | Class I | Active |
| Sterilex | 1000ml | FDA UDI | Class I | Active |
| SOLOMED Disposable Surgical Gown | Large Size | FDA UDI | Class I | Active |
| Pleura Med | Adult | FDA UDI | Class II | Active |
| Osto System | Neonatal | FDA UDI | Class I | Active |
| Pleura Med | Pediatric | FDA UDI | Class II | Active |
| Hidroderm | 15 x 21 cm | FDA UDI | Class I | Active |
| Flexmar | Small | FDA UDI | Class I | Active |
| Flexmar | Large | FDA UDI | Class I | Active |
| SOLOMED Disposable Surgical Gown | Extra Large Size | FDA UDI | Class I | Active |
| Bantex | 6cm | FDA UDI | Class I | Active |
| Osto System | Pediatric | FDA UDI | Class I | Active |
| Bantex | 8cm | FDA UDI | Class I | Active |
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