Nelaton Catheter (UDI 26975946800077)
Manufactured by Changzhou Weite Medical Equipment Co.,Ltd.
Device Regulatory Overview
The Nelaton Catheter (Model/Catalog Number: CC Rev. 7.1: 2023-01-23) is a medical device manufactured by Changzhou Weite Medical Equipment Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification U01010502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CC Rev. 7.1: 2023-01-23
- Product Code / EMDN
- U01010502
- Device Name
- Nelaton catheter
- Database Sync Date
- 2026-08-09 16:45:40
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Nelaton Catheter?
The registered manufacturer of record for Nelaton Catheter is Changzhou Weite Medical Equipment Co.,Ltd..
What is the Primary UDI-DI identifier for Nelaton Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26975946800077.
What classification code is assigned to this device?
This device is registered under product classification code U01010502.
Similar Classification Devices (U01010502)
Other Devices by Changzhou Weite Medical Equipment Co.,Ltd.
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