gudid
Primary ID: K-955.F&T
Foster & Thrive (UDI K-955.F&T)
Manufactured by MCKESSON CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Foster & Thrive - Primary ID K-955.F&T
Device Regulatory Overview
The Foster & Thrive (Model/Catalog Number: K-955.F&T) is a medical device manufactured by MCKESSON CORPORATION. This product is indexed under FDA Product Code / Category Classification FLL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K-955.F&T
- Product Code / EMDN
- FLL
- Device Name
- 50 pack of probe covers. A device intended to be used as a physical barrier between the patient and the probe of a thermometer to prevent cross-contamination between patients. This is a single-use device.
- Database Sync Date
- 2026-08-09 09:00:34
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 Foster & Thrive?
The registered manufacturer of record for Foster & Thrive is MCKESSON CORPORATION.
What is the Primary UDI-DI identifier for Foster & Thrive?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is K-955.F&T.
What classification code is assigned to this device?
This device is registered under product classification code FLL.
Similar Classification Devices (FLL)
Other Devices by MCKESSON CORPORATION
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