gudid
Primary ID: 00001000311R
ACL ELITE PRO (UDI 00001000311R)
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 PRO - Primary ID 00001000311R
Device Regulatory Overview
The ACL ELITE PRO (Model/Catalog Number: 00001000311R) 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
- 00001000311R
- Product Code / EMDN
- JPA
- Device Name
- ACL ELITE PRO (Refurbished)
- 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 PRO?
The registered manufacturer of record for ACL ELITE PRO is INSTRUMENTATION LABORATORY COMPANY.
What is the Primary UDI-DI identifier for ACL ELITE PRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00001000311R.
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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