eudamed_udi
Primary ID: 08058964720092
G1A 40 (UDI 08058964720092)
Manufactured by G21 S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for G1A 40 - Primary ID 08058964720092
Device Regulatory Overview
The G1A 40 (Model/Catalog Number: 800007) is a medical device manufactured by G21 S.R.L.. This product is indexed under FDA Product Code / Category Classification P099001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 800007
- Product Code / EMDN
- P099001
- Device Name
- G1A 40
- Database Sync Date
- 2026-08-09 18:55:50
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 G1A 40?
The registered manufacturer of record for G1A 40 is G21 S.R.L..
What is the Primary UDI-DI identifier for G1A 40?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058964720092.
What classification code is assigned to this device?
This device is registered under product classification code P099001.
Similar Classification Devices (P099001)
Other Devices by G21 S.R.L.
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