eudamed_udi
Primary ID: 08435723004837
Unspecified Brand (UDI 08435723004837)
Manufactured by MEDICAL PRECISION IMPLANTS, S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08435723004837
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: CM601 HG2) is a medical device manufactured by MEDICAL PRECISION IMPLANTS, S.A.. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CM601 HG2
- Product Code / EMDN
- Q010299
- Device Name
- Ti-Base
- Database Sync Date
- 2026-08-09 16:28:57
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 MEDICAL PRECISION IMPLANTS, S.A..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435723004837.
What classification code is assigned to this device?
This device is registered under product classification code Q010299.
Similar Classification Devices (Q010299)
Other Devices by MEDICAL PRECISION IMPLANTS, S.A.
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