gudid
Primary ID: QUICKPIN
QUICKPIN (UDI QUICKPIN)
Manufactured by LABORATORIOS GRIFOLS SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for QUICKPIN - Primary ID QUICKPIN
Device Regulatory Overview
The QUICKPIN (Model/Catalog Number: QUICKPIN) 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
- QUICKPIN
- Product Code / EMDN
- LHI
- Device Name
- QUICKPIN is a luer-lock spike used in manual or automated pharmacy compounding for addition and/or extraction of IV substances from rubber stoppered containers including multi-dose vials.
- Database Sync Date
- 2026-08-09 09:10:50
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 QUICKPIN?
The registered manufacturer of record for QUICKPIN is LABORATORIOS GRIFOLS SA.
What is the Primary UDI-DI identifier for QUICKPIN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is QUICKPIN.
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
Programmatic Export
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