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Sign in to claim this brandHangzhou Jimushi Meditech Co., Ltd.
US
Last updated May 30, 2026
What Hangzhou Jimushi Meditech Co., Ltd. makes
The company manufactures single-use intermittent urethral drainage catheters without antimicrobial coatings, designed for temporary urinary catheterization.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
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 Hangzhou Jimushi Meditech Co., Ltd. manufacture?
Hangzhou Jimushi Meditech Co., Ltd. specializes in intermittent urethral drainage catheters that are non-antimicrobial and intended for single-use. These catheters are designed for temporary urinary catheterization, meaning they are used for short-term drainage of urine from the bladder.
Where is Hangzhou Jimushi Meditech Co., Ltd. based?
Hangzhou Jimushi Meditech Co., Ltd. is based in the United States. The company’s location is relevant for understanding its regulatory oversight and compliance with U.S. medical device standards.
Which regulatory registries list the devices manufactured by Hangzhou Jimushi Meditech Co., Ltd.?
The devices produced by Hangzhou Jimushi Meditech Co., Ltd. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability.
How are the devices manufactured by Hangzhou Jimushi Meditech Co., Ltd. classified under FDA regulations?
The intermittent urethral drainage catheters produced by Hangzhou Jimushi Meditech Co., Ltd. fall under Class II classification according to FDA regulations. This classification is assigned based on the level of risk associated with the device, where Class II devices require special controls in addition to general controls to ensure safety and effectiveness.
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
- 413190154
Catalogue (57)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BeneCath® | NC16MC | FDA UDI | Class II | Active |
| BeneCath® | NCH10F | FDA UDI | Class II | Active |
| BeneCath® | NCW16M | FDA UDI | Class II | Active |
| BeneCath® | NC10F | FDA UDI | Class II | Active |
| BeneCath® | NC18MC | FDA UDI | Class II | Active |
| BeneCath® | NCW08P | FDA UDI | Class II | Active |
| BeneCath® | NCH14F | FDA UDI | Class II | Active |
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