eudamed_udi
Primary ID: 08058964726063
SpaceFlex Shoulder (UDI 08058964726063)
Manufactured by G21 S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SpaceFlex Shoulder - Primary ID 08058964726063
Device Regulatory Overview
The SpaceFlex Shoulder (Model/Catalog Number: 900001 12 42 15) is a medical device manufactured by G21 S.R.L.. This product is indexed under FDA Product Code / Category Classification P09010403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 900001 12 42 15
- Product Code / EMDN
- P09010403
- Device Name
- SpaceFlex Shoulder
- Database Sync Date
- 2026-08-09 16:48:04
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 SpaceFlex Shoulder?
The registered manufacturer of record for SpaceFlex Shoulder is G21 S.R.L..
What is the Primary UDI-DI identifier for SpaceFlex Shoulder?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058964726063.
What classification code is assigned to this device?
This device is registered under product classification code P09010403.
Similar Classification Devices (P09010403)
Other Devices by G21 S.R.L.
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