gudid
Primary ID: 00000880311
ACL ELITE (UDI 00000880311)
Manufactured by INSTRUMENTATION LABORATORY COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACL ELITE - Primary ID 00000880311
Device Regulatory Overview
The ACL ELITE (Model/Catalog Number: 00000880311) is a medical device manufactured by INSTRUMENTATION LABORATORY COMPANY. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00000880311
- Product Code / EMDN
- JPA
- Device Name
- ACL ELITE
- Database Sync Date
- 2026-08-09 09:10:50
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 ACL ELITE?
The registered manufacturer of record for ACL ELITE is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for ACL ELITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00000880311.
What classification code is assigned to this device?
This device is registered under product classification code JPA.
Similar Classification Devices (JPA)
Other Devices by INSTRUMENTATION LABORATORY COMPANY
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