gudid
Primary ID: 66020961
Renasys (UDI 66020961)
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 - Primary ID 66020961
Device Regulatory Overview
The Renasys (Model/Catalog Number: 66020961) 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
- 66020961
- Product Code / EMDN
- OMP
- Device Name
- The RENASYS Procedure Packs are intended to be used in conjunction with Smith & Nephew NPWT systems. Smith & Nephew NPWT systems are indicated for patients who would benefit from a suction device (negative pressure wound therapy) as it may promote wound healing via the removal of fluids, including irrigation and body fluids, wound exudates and infectious materials. Examples of appropriate wound types include: chronic, acute, traumatic, sub-acute and dehisced wounds, ulcers (such as pressure or diabetic), partial-thickness burns, flaps and grafts.
- Database Sync Date
- 2026-08-09 09:08:52
Full Regulatory Attributes
🔒 Token Gated
{
"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?
The registered manufacturer of record for Renasys is SMITH & NEPHEW MEDICAL LIMITED.
What is the Primary UDI-DI identifier for Renasys?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66020961.
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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