gudid
Primary ID: 66021739
RENASYS GO (UDI 66021739)
Manufactured by SMITH & NEPHEW MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RENASYS GO - Primary ID 66021739
Device Regulatory Overview
The RENASYS GO (Model/Catalog Number: 66021739) is a medical device manufactured by SMITH & NEPHEW MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification OMP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 66021739
- Product Code / EMDN
- OMP
- Device Name
- Clinician User Manual US Only
- Database Sync Date
- 2026-08-09 09:08:52
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 RENASYS GO?
The registered manufacturer of record for RENASYS GO is SMITH & NEPHEW MEDICAL LIMITED.
What is the Primary UDI-DI identifier for RENASYS GO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66021739.
What classification code is assigned to this device?
This device is registered under product classification code OMP.
Similar Classification Devices (OMP)
Other Devices by SMITH & NEPHEW MEDICAL LIMITED
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