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Trident(TM) Endoscopic Ultrasound Biopsy Needle (FNB)

FDA UDI

Class II (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
Trident(TM) Endoscopic Ultrasound Biopsy Needle (FNB) FDA UDI
Generic Name
Ultrasound aspiration biopsy procedure kit FDA UDI
Device Name
Maximum insertion portion diameter:2.3mm,Needle:19G,Maximum needle length:80mm,Working channel: Greater than or equal to 2.8mm,Working Length:1197~1237mm, FNB needle FDA UDI
Model / Reference
EUS-19-1-CS1 FDA UDI
Description
Maximum insertion portion diameter:2.3mm,Needle:19G,Maximum needle length:80mm,Working channel: Greater than or equal to 2.8mm,Working Length:1197~1237mm, FNB needle FDA UDI

Identifiers

Primary DI / UDI-DI
06932503534758 FDA UDI
510(k) Number
K172309 FDA UDI
FDA Product Code
FCG FDA UDI
GMDN Term
Ultrasound aspiration biopsy procedure kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 19 Gauge FDA UDI

Category: Ultrasound aspiration biopsy procedure kit

Trident(TM) Endoscopic Ultrasound Biopsy Needle (FNB) by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Ultrasound aspiration biopsy procedure kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2ff6d3da-8ac3-445e-acdb-608e0154a54b 36 fields · synced May 30, 2026