gudid
Primary ID: PB2SE
PhotonBlade with Adaptive Smoke Evacuation (UDI PB2SE)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PhotonBlade with Adaptive Smoke Evacuation - Primary ID PB2SE
Device Regulatory Overview
The PhotonBlade with Adaptive Smoke Evacuation (Model/Catalog Number: PB2SE) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PB2SE
- Product Code / EMDN
- GEI
- Device Name
- The PhotonBlade with Adaptive Smoke Evacuation is a monopolar RF device coupled with illumination that is indicated for cutting and coagulation of tissue during general surgical procedures and for removing 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 PhotonBlade with Adaptive Smoke Evacuation?
The registered manufacturer of record for PhotonBlade with Adaptive Smoke Evacuation is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for PhotonBlade with Adaptive Smoke Evacuation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PB2SE.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Other Devices by STRYKER CORPORATION
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