gudid
Primary ID: MT200
Maxithins (UDI MT200)
Manufactured by TRANZONIC COMPANIES, THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Maxithins - Primary ID MT200
Device Regulatory Overview
The Maxithins (Model/Catalog Number: MT200) is a medical device manufactured by TRANZONIC COMPANIES, THE. This product is indexed under FDA Product Code / Category Classification HHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MT200
- Product Code / EMDN
- HHD
- Device Name
- MAXITHINS REGULAR MAXI W/WINGS VEND PACK 200/CS
- Database Sync Date
- 2026-08-09 09:08:46
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 Maxithins?
The registered manufacturer of record for Maxithins is TRANZONIC COMPANIES, THE.
What is the Primary UDI-DI identifier for Maxithins?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MT200.
What classification code is assigned to this device?
This device is registered under product classification code HHD.
Similar Classification Devices (HHD)
Other Devices by TRANZONIC COMPANIES, THE
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