gudid
Primary ID: BDASD02
Aptra (UDI BDASD02)
Manufactured by Ningbo Wise Optomech Technology Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aptra - Primary ID BDASD02
Device Regulatory Overview
The Aptra (Model/Catalog Number: BDASD02) is a medical device manufactured by Ningbo Wise Optomech Technology Corporation. This product is indexed under FDA Product Code / Category Classification FGB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BDASD02
- Product Code / EMDN
- FGB
- Device Name
- Single-Use Digital Flexible Ureteroscope
- Database Sync Date
- 2026-08-09 09:00:28
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 Aptra?
The registered manufacturer of record for Aptra is Ningbo Wise Optomech Technology Corporation.
What is the Primary UDI-DI identifier for Aptra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BDASD02.
What classification code is assigned to this device?
This device is registered under product classification code FGB.
Similar Classification Devices (FGB)
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