eudamed_udi
Primary ID: 05051986011776
355mm Taper Wave Prestige (UDI 05051986011776)
Manufactured by Surgical Innovations Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 355mm Taper Wave Prestige - Primary ID 05051986011776
Device Regulatory Overview
The 355mm Taper Wave Prestige (Model/Catalog Number: 101-49048) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L180802 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101-49048
- Product Code / EMDN
- L180802
- Device Name
- 355mm Taper Wave Prestige
- Database Sync Date
- 2026-08-09 19:03:23
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 355mm Taper Wave Prestige?
The registered manufacturer of record for 355mm Taper Wave Prestige is Surgical Innovations Ltd..
What is the Primary UDI-DI identifier for 355mm Taper Wave Prestige?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986011776.
What classification code is assigned to this device?
This device is registered under product classification code L180802.
Similar Classification Devices (L180802)
Other Devices by Surgical Innovations Ltd.
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