eudamed_udi
Primary ID: 06980251807013
MANUAL BED (UDI 06980251807013)
Manufactured by FOSHAN DAX MEDICAL EQUIPMENT CO., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MANUAL BED - Primary ID 06980251807013
Device Regulatory Overview
The MANUAL BED (Model/Catalog Number: DX-101T) is a medical device manufactured by FOSHAN DAX MEDICAL EQUIPMENT CO., LTD. This product is indexed under FDA Product Code / Category Classification V080602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DX-101T
- Product Code / EMDN
- V080602
- Device Name
- MANUAL BED
- Database Sync Date
- 2026-08-09 16:28:51
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 MANUAL BED?
The registered manufacturer of record for MANUAL BED is FOSHAN DAX MEDICAL EQUIPMENT CO., LTD.
What is the Primary UDI-DI identifier for MANUAL BED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06980251807013.
What classification code is assigned to this device?
This device is registered under product classification code V080602.
Similar Classification Devices (V080602)
Other Devices by FOSHAN DAX MEDICAL EQUIPMENT CO., LTD
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