eudamed_udi
Primary ID: 08052532834082
SCREW FOR CUP (UDI 08052532834082)
Manufactured by Adler Ortho S.p.A
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCREW FOR CUP - Primary ID 08052532834082
Device Regulatory Overview
The SCREW FOR CUP (Model/Catalog Number: 0761135) is a medical device manufactured by Adler Ortho S.p.A. This product is indexed under FDA Product Code / Category Classification P09088007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0761135
- Product Code / EMDN
- P09088007
- Device Name
- OMNIA GUIDED SCREW HA COATED DIAM 8,5; L. 35 mm
- Database Sync Date
- 2026-08-09 16:29:53
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 SCREW FOR CUP?
The registered manufacturer of record for SCREW FOR CUP is Adler Ortho S.p.A.
What is the Primary UDI-DI identifier for SCREW FOR CUP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052532834082.
What classification code is assigned to this device?
This device is registered under product classification code P09088007.
Similar Classification Devices (P09088007)
Other Devices by Adler Ortho S.p.A
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