gudid
Primary ID: -
GRI-FILL (UDI -)
Manufactured by LABORATORIOS GRIFOLS SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GRI-FILL - Primary ID -
Device Regulatory Overview
The GRI-FILL (Model/Catalog Number: -) is a medical device manufactured by LABORATORIOS GRIFOLS SA. This product is indexed under FDA Product Code / Category Classification NEP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- -
- Product Code / EMDN
- NEP
- Device Name
- GRI-FILL is a pharmacy compounding device (PCD) and as such is an electromechanical device controlled by software intended to deliver a specified concentration or proportion of ingredients different from the initial solutions.
- Database Sync Date
- 2026-08-09 09:10:50
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of GRI-FILL?
The registered manufacturer of record for GRI-FILL is LABORATORIOS GRIFOLS SA.
What is the Primary UDI-DI identifier for GRI-FILL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is -.
What classification code is assigned to this device?
This device is registered under product classification code NEP.
Similar Classification Devices (NEP)
Other Devices by LABORATORIOS GRIFOLS SA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint