gudid
Primary ID: A135TSE
Eikon LT Adapt Smoke Evacuation (UDI A135TSE)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eikon LT Adapt Smoke Evacuation - Primary ID A135TSE
Device Regulatory Overview
The Eikon LT Adapt Smoke Evacuation (Model/Catalog Number: A135TSE) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification GAD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A135TSE
- Product Code / EMDN
- GAD
- Device Name
- Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system.
- Database Sync Date
- 2026-08-09 09:31:28
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 Eikon LT Adapt Smoke Evacuation?
The registered manufacturer of record for Eikon LT Adapt Smoke Evacuation is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for Eikon LT Adapt Smoke Evacuation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A135TSE.
What classification code is assigned to this device?
This device is registered under product classification code GAD.
Similar Classification Devices (GAD)
Other Devices by STRYKER CORPORATION
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