ELBOW CRUTCHES (UDI Y12030601)
Device Regulatory Overview
The ELBOW CRUTCHES (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Y12030601
- Device Name
- ELBOW CRUTCHES
- Database Sync Date
- 2026-08-09 16:18:37
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 ELBOW CRUTCHES?
The registered manufacturer of record for ELBOW CRUTCHES is .
What is the Primary UDI-DI identifier for ELBOW CRUTCHES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Y12030601.
What classification code is assigned to this device?
This device is registered under product classification code Y12030601.
Similar Classification Devices (Y12030601)
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