gudid
Primary ID: InBody970S
InBody (UDI InBody970S)
Manufactured by InBody Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for InBody - Primary ID InBody970S
Device Regulatory Overview
The InBody (Model/Catalog Number: InBody970S) is a medical device manufactured by InBody Co., Ltd.. This product is indexed under FDA Product Code / Category Classification PUH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- InBody970S
- Product Code / EMDN
- PUH
- Device Name
- Body Composition Analyzer, Exempt
- Database Sync Date
- 2026-08-09 09:52:00
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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Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of InBody?
The registered manufacturer of record for InBody is InBody Co., Ltd..
What is the Primary UDI-DI identifier for InBody?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is InBody970S.
What classification code is assigned to this device?
This device is registered under product classification code PUH.
Similar Classification Devices (PUH)
Other Devices by InBody Co., Ltd.
Programmatic Export
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