gudid
Primary ID: 2 ways
SET GRI-FILL 3.0 (UDI 2 ways)
Manufactured by LABORATORIOS GRIFOLS SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SET GRI-FILL 3.0 - Primary ID 2 ways
Device Regulatory Overview
The SET GRI-FILL 3.0 (Model/Catalog Number: 2 ways) is a medical device manufactured by LABORATORIOS GRIFOLS SA. This product is indexed under FDA Product Code / Category Classification LHI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2 ways
- Product Code / EMDN
- LHI
- Device Name
- SETS GRI-FILL 3.0 are fluid transfer sets for use with the GRI-FILL 3.0 pharmacy compounding device in order to compound or mix different multi-ingredient solutions and to channel them into a final suitable IV container. The set is a disposable component of the compounding device. The 1 WAY / 2 WAY models are made up of a syringe, a distributor, tubing to channel the fluid and a waste/residue bag. Sets are available for 1 or 2 source substances. Also a Luer female - female adapter is available as an accessory to the 1 or 2 way transfer sets. The MULTIPLE model is also used as an accessory with the 1IWAY I 2WAY sets for channeling the same solution from up to six (6) source containers delivering them into a final IV container. It is made up of connectors and tubing to enable interconnection of the different source containers.
- 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
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SET GRI-FILL 3.0?
The registered manufacturer of record for SET GRI-FILL 3.0 is LABORATORIOS GRIFOLS SA.
What is the Primary UDI-DI identifier for SET GRI-FILL 3.0?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2 ways.
What classification code is assigned to this device?
This device is registered under product classification code LHI.
Similar Classification Devices (LHI)
Other Devices by LABORATORIOS GRIFOLS SA
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