RALLY (UDI 71271570)
Manufactured by Smith & Nephew, Inc.
Device Regulatory Overview
The RALLY (Model/Catalog Number: 71271570) is a medical device manufactured by Smith & Nephew, Inc.. This product is indexed under FDA Product Code / Category Classification LOD 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
- 71271570
- Product Code / EMDN
- LOD
- Device Name
- RALLY HV AB BONE CEMENT 40 GRAMS
- Database Sync Date
- 2026-08-09 09:52:31
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 RALLY?
The registered manufacturer of record for RALLY is Smith & Nephew, Inc..
What is the Primary UDI-DI identifier for RALLY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71271570.
What classification code is assigned to this device?
This device is registered under product classification code LOD.
Similar Classification Devices (LOD)
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