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Sign in to claim this brandPHARMA SEPT MEDICAL PRODUCTS (1995) LTD.
US
Last updated May 23, 2026
What PHARMA SEPT MEDICAL PRODUCTS (1995) LTD. makes
The company manufactures single-use protective drapes and coverings for medical equipment, including microscope drapes for specific brands like Zeiss and Leica, as well as covers for video cameras, C-arms, and X-ray imaging systems. These products are designed to maintain sterility and prevent contamination during procedures, with variations in size and material to fit different device models.
All listed devices fall under Class I regulatory classification in the U.S., meaning they are subject to general controls without requiring pre-market approval. The products are registered in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The manufacturer 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 Pharma Sept Medical Products manufacture?
Pharma Sept Medical Products specializes in single-use protective drapes and coverings for medical equipment. Their products include microscope drapes tailored for specific brands like Zeiss and Leica, as well as covers for video cameras, C-arms, and X-ray imaging systems. These items are designed to maintain sterility and prevent contamination during medical procedures.
Where is Pharma Sept Medical Products based?
The company is based in the United States. This location aligns with its focus on compliance with U.S. medical device regulations, including registration in the FDA’s Unique Device Identifier (UDI) database.
Which regulatory registries list Pharma Sept Medical Products’ devices?
Pharma Sept Medical Products’ devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and compliance for medical devices in the U.S., helping track and monitor products throughout their lifecycle.
How are Pharma Sept Medical Products’ devices classified under U.S. regulations?
All of Pharma Sept Medical Products’ listed devices fall under Class I regulatory classification in the U.S. This classification means they are subject to general controls, such as good manufacturing practices and labeling requirements, but do not require pre-market approval. Class I devices are typically considered low-risk.
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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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 532186541
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