Plum (UDI 1966128)
Manufactured by ICU Medical, Inc.
Device Regulatory Overview
The Plum (Model/Catalog Number: 1966128) is a medical device manufactured by ICU Medical, Inc.. This product is indexed under FDA Product Code / Category Classification FPA within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump...
Plum Duo Infusion Pump, 40002-0401...
Plum Duo Precision IV Pump, 40002-0403...
Technical Specifications
- Model Number
- 1966128
- Product Code / EMDN
- FPA
- Device Name
- LIFESHIELD LATEX-FREE 150 ML BURETTE PLUMSET CONVERTIBLE PIERCING PIN, 154 INCH PREPIERCED INJECTION SITES & OPTION-LOK, NON-DEHP
- Database Sync Date
- 2026-08-09 09:39:02
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 Plum?
The registered manufacturer of record for Plum is ICU Medical, Inc..
What is the Primary UDI-DI identifier for Plum?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1966128.
What classification code is assigned to this device?
This device is registered under product classification code FPA.
Similar Classification Devices (FPA)
Other Devices by ICU Medical, Inc.
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