eudamed_udi
Primary ID: 08053876009075
Unspecified Brand (UDI 08053876009075)
Manufactured by NEW ANCORVIS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08053876009075
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: ANSM41E) is a medical device manufactured by NEW ANCORVIS SRL. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ANSM41E
- Product Code / EMDN
- Q010299
- Device Name
- Analogo da gesso - Analogue for plaster
- Database Sync Date
- 2026-08-09 16:28:53
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is NEW ANCORVIS SRL.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053876009075.
What classification code is assigned to this device?
This device is registered under product classification code Q010299.
Similar Classification Devices (Q010299)
Other Devices by NEW ANCORVIS SRL
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