eudamed_udi
Primary ID: 04711552923384
Anscare (UDI 04711552923384)
Manufactured by Cenefom Corp.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anscare - Primary ID 04711552923384
Device Regulatory Overview
The Anscare (Model/Catalog Number: NS-021-1) is a medical device manufactured by Cenefom Corp.. This product is indexed under FDA Product Code / Category Classification M040799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NS-021-1
- Product Code / EMDN
- M040799
- Device Name
- ENT Sponge
- Database Sync Date
- 2026-08-09 16:46:10
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 Anscare?
The registered manufacturer of record for Anscare is Cenefom Corp..
What is the Primary UDI-DI identifier for Anscare?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04711552923384.
What classification code is assigned to this device?
This device is registered under product classification code M040799.
Similar Classification Devices (M040799)
Other Devices by Cenefom Corp.
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