gudid
Primary ID: JT130400000
4F REGULAR COAXIAL DILATOR (UDI JT130400000)
Manufactured by JET MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 4F REGULAR COAXIAL DILATOR - Primary ID JT130400000
Device Regulatory Overview
The 4F REGULAR COAXIAL DILATOR (Model/Catalog Number: JT130400000) is a medical device manufactured by JET MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification MPB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- JT130400000
- Product Code / EMDN
- MPB
- Device Name
- Database Sync Date
- 2026-08-09 09:22:16
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 4F REGULAR COAXIAL DILATOR?
The registered manufacturer of record for 4F REGULAR COAXIAL DILATOR is JET MEDICAL, INC..
What is the Primary UDI-DI identifier for 4F REGULAR COAXIAL DILATOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is JT130400000.
What classification code is assigned to this device?
This device is registered under product classification code MPB.
Similar Classification Devices (MPB)
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