Rectal tube (UDI 26975946806154)
Manufactured by Changzhou Weite Medical Equipment Co.,Ltd.
Device Regulatory Overview
The Rectal tube (Model/Catalog Number: EN 12439:1998) is a medical device manufactured by Changzhou Weite Medical Equipment Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification G020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EN 12439:1998
- Product Code / EMDN
- G020301
- Device Name
- Rectal tube
- Database Sync Date
- 2026-08-09 16:46:12
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 Rectal tube?
The registered manufacturer of record for Rectal tube is Changzhou Weite Medical Equipment Co.,Ltd..
What is the Primary UDI-DI identifier for Rectal tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26975946806154.
What classification code is assigned to this device?
This device is registered under product classification code G020301.
Similar Classification Devices (G020301)
Other Devices by Changzhou Weite Medical Equipment Co.,Ltd.
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