eudamed_udi
Primary ID: 08436583730966
DG Spin (UDI 08436583730966)
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 Spin - Primary ID 08436583730966
Device Regulatory Overview
The DG Spin (Model/Catalog Number: 210363) is a medical device manufactured by Diagnostic Grifols, S.A.. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 210363
- Product Code / EMDN
- W02069003
- Device Name
- DG Spin
- Database Sync Date
- 2026-08-09 16:30:19
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 Spin?
The registered manufacturer of record for DG Spin is Diagnostic Grifols, S.A..
What is the Primary UDI-DI identifier for DG Spin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436583730966.
What classification code is assigned to this device?
This device is registered under product classification code W02069003.
Similar Classification Devices (W02069003)
Other Devices by Diagnostic Grifols, S.A.
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