Apex™

Apex, Control Module, TPN MGR - Asset

Registry build 21.09.26
2manufacturers in China registered for this device type
15catalogue numbers in this listing
3recalls on this code

Who Else Makes It

All of them in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NEP
Manufacturer City Province Registered as Device types
Yangzhou Xingwei Medical Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 5
Yangzhou Weideli Trading Co., Ltd. Yangzhou Jiangsu Contract manufacturer 10

Record

Regulatory record for Apex™
Listed by B. Braun Medical Inc., United States
FDA product code NEP
Device type System/Device, Pharmacy Compounding
Device class Class 2
Regulation 21 CFR 880.5440
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-09-23
Record revised 2025-02-24 (version 4)

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, serial number
Storage Special storage condition: Fragile, handle with care

Catalogue Numbers

Catalogue numbers for Apex™
Catalogue number Size Per pack Status
601224 In distribution
601223 In distribution
601237 In distribution
601228-99 In distribution
AX1000 In distribution
AX5000 In distribution
601240 In distribution
601227-99 In distribution
601227 In distribution
601224-99 In distribution
601220 In distribution
601239 In distribution
601238 In distribution
601241 In distribution
2112537 50 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Exactamix Baxter Healthcare Corporation 27
ICU Medical, Inc. ICU Medical, Inc 16
Pinnacle® B. Braun Medical Inc. 13
System/Device, Pharmacy Compounding Baxter Healthcare Corporation 9
DianaTM Compounding Workflow System ICU Medical, Inc 9
Repeater Baxter Healthcare Corporation 8
DianaTM Automated Drug Compounding System ICU Medical, Inc 5
Single Lead High Volume Pump Chamber SET MPS Pharma & Medical, Inc. 4
Abacus Baxter Healthcare Corporation 4
Apoteca AEA SRL 3
GRI-BAG Laboratorios Grifols SA 3
Exactamix Baxter Corporation Englewood 3

Showing 12 of 35. All products under System/Device, Pharmacy Compounding

Recalls

3 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
2020-11-23 Class II Software change control There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that 248 units 2023-03-14
2020-11-23 Class II Software change control There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that 16 units 2023-03-14
2020-11-23 Class II Software change control There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that 85 units 2023-03-14

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