gudid
Primary ID: A2
Bovie (UDI A2)
Manufactured by ASPEN SURGICAL PRODUCTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bovie - Primary ID A2
Device Regulatory Overview
The Bovie (Model/Catalog Number: A2) is a medical device manufactured by ASPEN SURGICAL PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification LXE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A2
- Product Code / EMDN
- LXE
- Device Name
- ACUDOP LL 2MHZ OB PROBE (ONLY)
- Database Sync Date
- 2026-08-09 09:31:02
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 Bovie?
The registered manufacturer of record for Bovie is ASPEN SURGICAL PRODUCTS, INC..
What is the Primary UDI-DI identifier for Bovie?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A2.
What classification code is assigned to this device?
This device is registered under product classification code LXE.
Similar Classification Devices (LXE)
Other Devices by ASPEN SURGICAL PRODUCTS, INC.
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