eudamed_udi
Primary ID: 04751040972517
Acupressure Octopus High lumbar orthosis (UDI 04751040972517)
Manufactured by AGM orthopaedics
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acupressure Octopus High lumbar orthosis - Primary ID 04751040972517
Device Regulatory Overview
The Acupressure Octopus High lumbar orthosis (Model/Catalog Number: 100HL0202L) is a medical device manufactured by AGM orthopaedics. This product is indexed under FDA Product Code / Category Classification Y060306 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100HL0202L
- Product Code / EMDN
- Y060306
- Device Name
- Acupressure Octopus spinal orthosis
- Database Sync Date
- 2026-08-09 17:06:19
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 Acupressure Octopus High lumbar orthosis?
The registered manufacturer of record for Acupressure Octopus High lumbar orthosis is AGM orthopaedics.
What is the Primary UDI-DI identifier for Acupressure Octopus High lumbar orthosis?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04751040972517.
What classification code is assigned to this device?
This device is registered under product classification code Y060306.
Similar Classification Devices (Y060306)
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