eudamed_udi
Primary ID: D-ARMF000017203PPE35031G7
OSTEOPLUS (UDI D-ARMF000017203PPE35031G7)
Manufactured by STEELDEC SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OSTEOPLUS - Primary ID D-ARMF000017203PPE35031G7
Device Regulatory Overview
The OSTEOPLUS (Model/Catalog Number: PPE.3503) is a medical device manufactured by STEELDEC SA. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PPE.3503
- Product Code / EMDN
- Q010280
- Device Name
- UCLA CALCINABLE BASE METALICA PLATAFORMA 3,45 SIN HEXÁGONO SHe
- Database Sync Date
- 2026-08-09 17:08:32
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 OSTEOPLUS?
The registered manufacturer of record for OSTEOPLUS is STEELDEC SA.
What is the Primary UDI-DI identifier for OSTEOPLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ARMF000017203PPE35031G7.
What classification code is assigned to this device?
This device is registered under product classification code Q010280.
Similar Classification Devices (Q010280)
Other Devices by STEELDEC SA
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