eudamed_udi
Primary ID: 06972091928553
BM Rectal Catheters (UDI 06972091928553)
Manufactured by Bonree Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BM Rectal Catheters - Primary ID 06972091928553
Device Regulatory Overview
The BM Rectal Catheters (Model/Catalog Number: 50836002) is a medical device manufactured by Bonree Medical 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
- 50836002
- Product Code / EMDN
- G020301
- Device Name
- Rectal Catheters
- Database Sync Date
- 2026-08-09 16:48:51
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 BM Rectal Catheters?
The registered manufacturer of record for BM Rectal Catheters is Bonree Medical Co., Ltd..
What is the Primary UDI-DI identifier for BM Rectal Catheters?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972091928553.
What classification code is assigned to this device?
This device is registered under product classification code G020301.
Similar Classification Devices (G020301)
Other Devices by Bonree Medical Co., Ltd.
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