eudamed_udi
Primary ID: 08058964727886
Flex Drill (UDI 08058964727886)
Manufactured by G21 S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flex Drill - Primary ID 08058964727886
Device Regulatory Overview
The Flex Drill (Model/Catalog Number: 900212) is a medical device manufactured by G21 S.R.L.. This product is indexed under FDA Product Code / Category Classification K010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 900212
- Product Code / EMDN
- K010302
- Device Name
- Flex Drill
- Database Sync Date
- 2026-08-09 18:46:35
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 Flex Drill?
The registered manufacturer of record for Flex Drill is G21 S.R.L..
What is the Primary UDI-DI identifier for Flex Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058964727886.
What classification code is assigned to this device?
This device is registered under product classification code K010302.
Similar Classification Devices (K010302)
Other Devices by G21 S.R.L.
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