gudid
Primary ID: 0163273
35X-IT ProFlexx Incubator Transporter (UDI 0163273)
Manufactured by FERNO-WASHINGTON, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 35X-IT ProFlexx Incubator Transporter - Primary ID 0163273
Device Regulatory Overview
The 35X-IT ProFlexx Incubator Transporter (Model/Catalog Number: 0163273) is a medical device manufactured by FERNO-WASHINGTON, INC.. This product is indexed under FDA Product Code / Category Classification FPO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0163273
- Product Code / EMDN
- FPO
- Device Name
- 35X-IT ProFlexx Incubator Transporter, Red w/Dropframe
- Database Sync Date
- 2026-08-09 09:09:20
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 35X-IT ProFlexx Incubator Transporter?
The registered manufacturer of record for 35X-IT ProFlexx Incubator Transporter is FERNO-WASHINGTON, INC..
What is the Primary UDI-DI identifier for 35X-IT ProFlexx Incubator Transporter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0163273.
What classification code is assigned to this device?
This device is registered under product classification code FPO.
Similar Classification Devices (FPO)
Other Devices by FERNO-WASHINGTON, INC.
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