Trident(TM) Adapt Endoscopic Ultrasound Biopsy Needle(FNB) (UDI EUS-19-1-F)
Manufactured by Micro-Tech (Nanjing) Co., Ltd.
Device Regulatory Overview
The Trident(TM) Adapt Endoscopic Ultrasound Biopsy Needle(FNB) (Model/Catalog Number: EUS-19-1-F) is a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification ODG within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- EUS-19-1-F
- Product Code / EMDN
- ODG
- Device Name
- Maximum insertion portion diameter:2.5mm,Needle:19G,Maximum needle length.
- Database Sync Date
- 2026-08-09 09:24:49
Full Regulatory Attributes
🔒 Token Gated
{
"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 Trident(TM) Adapt Endoscopic Ultrasound Biopsy Needle(FNB)?
The registered manufacturer of record for Trident(TM) Adapt Endoscopic Ultrasound Biopsy Needle(FNB) is Micro-Tech (Nanjing) Co., Ltd..
What is the Primary UDI-DI identifier for Trident(TM) Adapt Endoscopic Ultrasound Biopsy Needle(FNB)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EUS-19-1-F.
What classification code is assigned to this device?
This device is registered under product classification code ODG.
Similar Classification Devices (ODG)
Other Devices by Micro-Tech (Nanjing) Co., Ltd.
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