eudamed_udi
Primary ID: 08058964726261
PicoMix Syringe 180g (UDI 08058964726261)
Manufactured by G21 S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PicoMix Syringe 180g - Primary ID 08058964726261
Device Regulatory Overview
The PicoMix Syringe 180g (Model/Catalog Number: 900123-1) is a medical device manufactured by G21 S.R.L.. This product is indexed under FDA Product Code / Category Classification P099002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 900123-1
- Product Code / EMDN
- P099002
- Device Name
- PicoMix Syringe 180g
- Database Sync Date
- 2026-08-09 17:58:43
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 PicoMix Syringe 180g?
The registered manufacturer of record for PicoMix Syringe 180g is G21 S.R.L..
What is the Primary UDI-DI identifier for PicoMix Syringe 180g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058964726261.
What classification code is assigned to this device?
This device is registered under product classification code P099002.
Similar Classification Devices (P099002)
Other Devices by G21 S.R.L.
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