gudid
Primary ID: 1002US
KIRO Fill US (UDI 1002US)
Manufactured by KIRO GRIFOLS SL.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIRO Fill US - Primary ID 1002US
Device Regulatory Overview
The KIRO Fill US (Model/Catalog Number: 1002US) is a medical device manufactured by KIRO GRIFOLS SL.. This product is indexed under FDA Product Code / Category Classification NEP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1002US
- Product Code / EMDN
- NEP
- Device Name
- KIRO Fill is an automated pharmacy compounding device (PCD) for the preparation of non-hazardous Compounded Sterile Preparations (CSPs). The device is intended to be used only by qualified pharmacy personnel.
- Database Sync Date
- 2026-08-09 09:41:12
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 KIRO Fill US?
The registered manufacturer of record for KIRO Fill US is KIRO GRIFOLS SL..
What is the Primary UDI-DI identifier for KIRO Fill US?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1002US.
What classification code is assigned to this device?
This device is registered under product classification code NEP.
Similar Classification Devices (NEP)
Other Devices by KIRO GRIFOLS SL.
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