Semi-automatic Disposable Biopsy Needle (UDI 06954414659412)
Manufactured by Canyon Medical Inc.
Device Regulatory Overview
The Semi-automatic Disposable Biopsy Needle (Model/Catalog Number: BN-2/141800-1) is a medical device manufactured by Canyon Medical Inc.. This product is indexed under FDA Product Code / Category Classification A0102010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BN-2/141800-1
- Product Code / EMDN
- A0102010101
- Device Name
- Semi-automatic Disposable Biopsy Needle
- Database Sync Date
- 2026-08-09 16:28:46
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 Semi-automatic Disposable Biopsy Needle?
The registered manufacturer of record for Semi-automatic Disposable Biopsy Needle is Canyon Medical Inc..
What is the Primary UDI-DI identifier for Semi-automatic Disposable Biopsy Needle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06954414659412.
What classification code is assigned to this device?
This device is registered under product classification code A0102010101.
Similar Classification Devices (A0102010101)
Other Devices by Canyon Medical Inc.
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