Cardinal Health

Needle Counter; Foam Block with Magnet; Box Lock; Blade Disarmer; NS; 20/40 Count

Registry build 21.09.26
105manufacturers in China registered for this device type
57catalogue numbers in this listing
9recalls on this code

Who Else Makes It

Concentrated in Jiangsu (28), Zhejiang (23), Shanghai (16). 20 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FSM
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai Joy Crown Industry Co., Ltd. Pu Dong New Area Shanghai Contract manufacturer 64
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Gcmedica Enterprise Ltd.(Wuxi) Wuxi Jiangsu Contract manufacturer 55
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Conod Medical Co., Limited Changshu Jiangsu Contract manufacturer 48
Jiangsu Jumao X-Care Medical Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 37
BH Medical Products Co., Ltd. Changzhou Jiangsu Contract manufacturer 37
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
Mobility Source Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 26
Guangdong Shunde LQX Health Technology Inc. Foshan Guangdong Contract manufacturer 24

Showing 12 of 105. All 105 manufacturers in China registered for Tray, Surgical, Instrument

Record

Regulatory record for Cardinal Health
Listed by Cardinal Health 200, LLC, United States
FDA product code FSM
Device type Tray, Surgical, Instrument
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2023-10-10
Record revised 2022-06-17 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Over the counter Yes
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Case of 48, case of 40, case of 56, case of 72, case of 30, case of 50
Distribution end date 2024-10-30
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Cardinal Health
Catalogue number Size Per pack Status
5M30M30N 192 In distribution
NC404SSTA In distribution
LB101SST In distribution
3FM20ANSB 200 In distribution
6F40M30MB3 96 In distribution
3FF80SSA In distribution
LB401SST In distribution
4FM100SBBL In distribution
3FM70SSA In distribution
NC404SST In distribution
LB702SST In distribution
NC404A 200 In distribution
2M10M10N 340 In distribution
3FM70NS 96 In distribution
3FM70SSACA In distribution
SSK9010A In distribution
200-16B In distribution
NI16-1058 In distribution
3MM60SSA In distribution
8F10M0LR 200 In distribution
LB701SST In distribution
3MM20SSA In distribution
3FM20SSACA In distribution
3MM30SSA In distribution
3MM20SSACA In distribution
3FM20SSA-V In distribution
LB102SST In distribution
3FM40SSA In distribution
HT9942667A In distribution
2M15M15N 340 In distribution
3FM20SSB In distribution
3FM20SSA In distribution
4F40F40N 96 In distribution
3FM40SSACA In distribution
7M10M0LR 96 In distribution
100-10B In distribution
LB703SST In distribution
200-20B In distribution
6F40MB30LR 96 In distribution
NC108SST In distribution
LB102 96 Withdrawn
LB701 96 Withdrawn
LB101 96 Withdrawn
NC108 96 Withdrawn
3MM60ANSA 192 Withdrawn
3FF80ANSA 96 Withdrawn
3MM30ANSA 340 Withdrawn
LB702 96 Withdrawn
3FM40ANSB 96 Withdrawn
LB401 200 Withdrawn
LB703 96 Withdrawn
4FM100BL 96 Withdrawn
LB402 200 Withdrawn
LB103 96 Withdrawn
200-16B-V Withdrawn
3MM20ANSA 340 Withdrawn
LB230 96 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
IMS HU-Friedy MFG Co., LLC 2,710
Tray, Surgical, Instrument Synthes Gmbh 1,052
Tray, Surgical, Instrument Medtronic Sofamor Danek, Inc. 1,012
Hu-Friedy MFG Co., LLC. HU-Friedy MFG Co., LLC 666
Aptus Medartis Inc. 588
Acumed Acumed LLC 566
Aesculap Aesculap AG 532
Sklar Sklar Corporation 465
Hu-Friedy HU-Friedy MFG Co., LLC 438
Nordent Manufacturing Inc Nordent Manufacturing Inc 429
Level ONE KLS-Martin L.P. 341
Bahadir USA Bahadir USA LLC 300

Showing 12 of 3,212. All products under Tray, Surgical, Instrument

Recalls

9 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 4FS30SSA: 7488; Cat. No. 4FS31SSA: 48; Cat. No. 4MM 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 3FA40SSA: 23,952; Cat. No. 3FM40SSA: 140,736 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 4FA70SSA: 1,248; Cat. No. 4FM70SSA: 43,920 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 3FA70SSA: 23,808; Cat. No. 3FM70SSA: 54,912 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 3FS60SSA: 7,560; Cat. No. 3FS61SSA: 14,184; Cat. No 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 4FA40SSA: 96; Cat. No. 4FM40SSA: 32,592 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 4FS60SSA: 576; Cat. No. 4FS61SSA: 14,760; Cat. No. 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 4FM100SSA: 4,464 2016-08-01
2012-12-18 Class II Package design/selection Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility. Cat. No. 3FF80SSA: 16224 2016-08-01

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