eudamed_udi
Primary ID: D-ARMF000017203DAC400M1ZS
OSTEOPLUS (UDI D-ARMF000017203DAC400M1ZS)
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-ARMF000017203DAC400M1ZS
Device Regulatory Overview
The OSTEOPLUS (Model/Catalog Number: DAC.400.M) is a medical device manufactured by STEELDEC SA. This product is indexed under FDA Product Code / Category Classification Q010399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DAC.400.M
- Product Code / EMDN
- Q010399
- Device Name
- DESTORNILLADOR CA CUADRADO 4 mm
- Database Sync Date
- 2026-08-09 16:51:56
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-ARMF000017203DAC400M1ZS.
What classification code is assigned to this device?
This device is registered under product classification code Q010399.
Similar Classification Devices (Q010399)
Other Devices by STEELDEC SA
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