gudid
Primary ID: AMTM705
ARMEDICA (UDI AMTM705)
Manufactured by ARMEDICA MANUFACTURING CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARMEDICA - Primary ID AMTM705
Device Regulatory Overview
The ARMEDICA (Model/Catalog Number: AMTM705) is a medical device manufactured by ARMEDICA MANUFACTURING CORP.. This product is indexed under FDA Product Code / Category Classification IOE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AMTM705
- Product Code / EMDN
- IOE
- Device Name
- LAMINATED PLATFORM MOUNTED, ELECTRIC 10 FT BARIATRIC PARALLEL BARS
- Database Sync Date
- 2026-08-09 09:06:23
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 ARMEDICA?
The registered manufacturer of record for ARMEDICA is ARMEDICA MANUFACTURING CORP..
What is the Primary UDI-DI identifier for ARMEDICA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AMTM705.
What classification code is assigned to this device?
This device is registered under product classification code IOE.
Similar Classification Devices (IOE)
Other Devices by ARMEDICA MANUFACTURING CORP.
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