BNX

Fine Needle Aspiration Needle

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (2), Zhejiang (1).

Chinese manufacturers registered for FDA product code FCG
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Suzhou Leapmed Healthcare Corporation Suzhou Jiangsu Contract manufacturer 3

Record

Regulatory record for BNX
Listed by Covidien LP, United States
FDA product code FCG
Device type Biopsy Needle
Device class Class 2
Regulation 21 CFR 876.1075
510(k) K103668
Record published 2016-09-24
Record revised 2025-11-24 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack_or_inner_pack of 5, case of 999
Sizes Needle gauge 22 to 25 G
Distribution end date 2025-08-19

Catalogue Numbers

Catalogue numbers for BNX
Catalogue number Size Status
N-25-05 Needle Gauge 25 G In distribution
DSN-22-02 Working Length,1380-1430,Millimeter;Minimum Channel Size,2.8,Millimeter; Withdrawn
DSN-25-02 Needle Gauge 25 G Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biopsybell Biopsybell SRL 227
Biopsybell SRL Biopsybell SRL 130
Medline Industries, Inc. Medline Industries, Inc. 98
Themy M.D.L. S.R.L. 61
SemiCut M.D.L. S.R.L. 46
Temno® Merit Medical Systems, Inc. 37
Temno Carefusion 2200, Inc. 36
CorVocet™ Merit Medical Systems, Inc. 34
Truguide Bard Peripheral Vascular, Inc. 31
Temno Evolution® Merit Medical Systems, Inc. 28
ClearTip Finemedix 25
Magnum Bard Peripheral Vascular, Inc. 22

Showing 12 of 115. All products under Biopsy Needle

Recalls Naming This Product

5 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of BNX
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Covidien 510(k) number 2017-02-08 Class II Nonconforming Material/Component Handle may break during use. 1,096 Units (total for all products) 2019-07-18
Covidien 510(k) number 2017-02-08 Class II Nonconforming Material/Component Handle may break during use. 1,096 Units (total for all products) 2019-07-18
Covidien 510(k) number 2017-02-08 Class II Nonconforming Material/Component Handle may break during use. 1,096 Units (total for all products) 2019-07-18
Covidien 510(k) number 2017-02-08 Class II Nonconforming Material/Component Handle may break during use. 1,096 Units (total for all products) 2019-07-18
Covidien 510(k) number 2017-02-08 Class II Nonconforming Material/Component Handle may break during use. 1,096 Units (total for all products) 2019-07-18

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer