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Sign in to claim this brandInternational Medical Development Corporation
US
Last updated May 24, 2026
What International Medical Development Corporation makes
International Medical Development Corporation manufactures single-use spinal needles designed for medical procedures involving the spinal column. These devices are intended for one-time use in clinical settings to facilitate spinal injections or diagnostic procedures.
The company’s spinal needles are classified as Class II medical devices under FDA regulations 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 International Medical Development Corporation primarily manufacture?
International Medical Development Corporation specializes in single-use spinal needles. These devices are specifically designed for medical procedures involving the spinal column, such as spinal injections or diagnostic tests. The focus on single-use spinal needles reflects a commitment to sterile, disposable solutions for clinical settings.
Where is International Medical Development Corporation based?
The company is headquartered in the United States. This location aligns with regulatory frameworks like the FDA, which governs the classification and listing of its devices in the U.S. market.
How are the devices manufactured by International Medical Development Corporation classified under regulatory standards?
The spinal needles produced by International Medical Development Corporation fall under Class II medical device classification according to FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
Are the devices produced by International Medical Development Corporation listed in any regulatory registries?
Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. Listing in the UDI system ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and other stakeholders to identify and track specific devices like the GERTIE MARX SPINAL N.
Why does the company’s focus on spinal needles matter for healthcare providers?
The company’s specialization in single-use spinal needles ensures sterile, contamination-free procedures, reducing infection risks in spinal injections or diagnostics. Single-use devices also eliminate the need for reprocessing, streamlining workflows in clinical settings while adhering to infection control best practices.
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
- 078483253
Catalogue (37)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Gertie Marx Spinal N | EP177 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM24101-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM24124-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25124-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | EP175 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25190176 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM22124-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25190-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM26124-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25101-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2270-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM27101-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25215177 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25160-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | EP176 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2450-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | EP1735 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2750-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM261241735 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2490-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25215-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM22150-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2550-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM26101-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM27150-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2690-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2790-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | FNB2090-I-8 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM27160-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2650-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2590-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2250-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM27124-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2550-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM2290-I | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM25160175 | FDA UDI | Class II | Active |
| Gertie Marx Spinal N | GM22190-I | FDA UDI | Class II | Active |
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