eudamed_udi
Primary ID: 08437014205671
DG Gel Sol (UDI 08437014205671)
Manufactured by Diagnostic Grifols, S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DG Gel Sol - Primary ID 08437014205671
Device Regulatory Overview
The DG Gel Sol (Model/Catalog Number: 210354) is a medical device manufactured by Diagnostic Grifols, S.A.. This product is indexed under FDA Product Code / Category Classification W0103020999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 210354
- Product Code / EMDN
- W0103020999
- Device Name
- DG Gel Sol
- Database Sync Date
- 2026-08-09 16:30:31
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 DG Gel Sol?
The registered manufacturer of record for DG Gel Sol is Diagnostic Grifols, S.A..
What is the Primary UDI-DI identifier for DG Gel Sol?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437014205671.
What classification code is assigned to this device?
This device is registered under product classification code W0103020999.
Similar Classification Devices (W0103020999)
Other Devices by Diagnostic Grifols, S.A.
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