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Sign in to claim this brandWhat SWANN-MORTON LIMITED makes
The company manufactures single-use surgical instruments, including manual scalpel blades and complete single-use scalpels designed for one-time medical procedures.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. The company 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 Swann-Morton Limited manufacture?
Swann-Morton Limited specializes in single-use surgical instruments, specifically manual scalpel blades and complete single-use scalpels. These devices are designed for one-time medical procedures, ensuring sterility and reducing the risk of cross-contamination in clinical settings.
Where is Swann-Morton Limited based?
Swann-Morton Limited operates from the United States. The company’s headquarters and manufacturing facilities are located within the country, though specific regional locations are not provided.
Which regulatory registries list Swann-Morton Limited’s devices?
Swann-Morton Limited’s devices are included in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify medical devices authorized for use in the United States, ensuring transparency and traceability in the healthcare supply chain.
How are Swann-Morton Limited’s devices classified under FDA regulations?
Swann-Morton Limited’s devices fall under Class I classification according to FDA regulations. This classification applies to devices posing minimal risk to patients, such as single-use surgical instruments like scalpels and blades, which are generally considered low-risk and subject to fewer regulatory controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- swann-morton.com
- —
- —
- [email protected]
- Phone
- +4401142344231
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 212397483
Catalogue (58)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Swann Morton Ltd. | No. 16 NON STERILE BLADES | FDA UDI | Class I | Active |
| Swann Morton Ltd. | Z SWANN MAJOR BLADES | FDA UDI | Class I | Unknown |
| Swann Morton Ltd. | No. 9 NON STERILE BLADES | FDA UDI | Class I | Active |
| Swann Morton Ltd. | No. 12D NON STERILE BLADES | FDA UDI | Class I | Unknown |
| Swann Morton Ltd. | ASR BULK No. 11 STAINLESS BLADES | FDA UDI | Class I | Unknown |
| Swann Morton Ltd. | No. 25 NON STERILE BLADES | FDA UDI | Class I | Unknown |
| Swann Morton Ltd. | No. 22A NON STERILE BLADES | FDA UDI | Class I | Active |
| Swann Morton Ltd. | No. 25A NON STERILE BLADES | FDA UDI | Class I | Unknown |
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