gudid
Primary ID: CTR001201S
MEDLINE (UDI CTR001201S)
Manufactured by MEDLINE INDUSTRIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDLINE - Primary ID CTR001201S
Device Regulatory Overview
The MEDLINE (Model/Catalog Number: CTR001201S) is a medical device manufactured by MEDLINE INDUSTRIES, INC.. This product is indexed under FDA Product Code / Category Classification MUI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CTR001201S
- Product Code / EMDN
- MUI
- Device Name
- GEL,ULTRASOUND,STRL,0.7-OZ,CLEAR,FOIL
- Database Sync Date
- 2026-08-09 09:38:40
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 MEDLINE?
The registered manufacturer of record for MEDLINE is MEDLINE INDUSTRIES, INC..
What is the Primary UDI-DI identifier for MEDLINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CTR001201S.
What classification code is assigned to this device?
This device is registered under product classification code MUI.
Similar Classification Devices (MUI)
Other Devices by MEDLINE INDUSTRIES, INC.
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