Medline

Cuff,bp,sm Adult,for 3001/4001/1001/5001

Registry build 21.09.26
98manufacturers in China registered for this device type
30catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (67), Jiangsu (11), Zhejiang (6). 17 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DXN
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Andon Health Co., Ltd. Tianjin Tianjin Contract manufacturer 22
Taizhou Rich Medical Products Co., Ltd. Taizhou Jiangsu Contract manufacturer 20
Medwell Technology Limited Dongguan Guangdong Contract manufacturer 10
Honsun (Nantong) Co., Ltd. Nantong Jiangsu Contract manufacturer 9
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9
Yahorng Dongguan Electronic Co Ltd Guangdong Guangdong Contract manufacturer 8
Guangzhou Daxin Health Technology (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 7
Omron (Dalian) Co., Ltd. (Plant 1) Dalian Liaoning Contract manufacturer 7
Wuhan Strong Electronics Wuhan Hubei Contract manufacturer 6
Dongguan Polygreen Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Shenzhen Brav Electronic Technologies Co., Ltd. Shenzhen Guangdong Contract manufacturer 3

Showing 12 of 98. All 98 manufacturers in China registered for System, Measurement, Blood-Pressure, Non-Invasive

Record

Regulatory record for Medline
Listed by Medline Industries, Inc., United States
FDA product code DXN
Device type System, Measurement, Blood-Pressure, Non-Invasive
Device class Class 2
Regulation 21 CFR 870.1130
510(k) K200939
Record published 2026-03-06
Record revised 2024-09-30 (version 5)

Specifications

Specifications
MRI safety MR Unsafe
Single use Yes
Prescription Prescription only
Over the counter Yes
Latex Labelled latex-free
Label carries lot or batch number, serial number
Storage Storage environment humidity 15 to 90 % RH; Special storage condition: Handle With Care; Keep Dry; Storage environment temperature -20 to 55 °C; Handling environment temperature 5 to 40 °C; Handling environment atmospheric pressure 70 to 106 KiloPascal; Handling environment humidity 15 to 90 % RH
Packaging Case of 36
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Medline
Catalogue number Size Status
MDSBPECON In distribution
MDS9773 In distribution
MDS9973 In distribution
MDS9972 In distribution
MDS5001 In distribution
MDS9970 In distribution
MDS7001B In distribution
MDSBPADVAN In distribution
MDS3002LA In distribution
MDS8001B In distribution
MDS9104 In distribution
MDS9971 In distribution
MDS3001U In distribution
MDS8001BXL In distribution
MDS3001LA In distribution
MDS1001CS In distribution
MDS4001 In distribution
MDS9108 In distribution
MDS9113 In distribution
MDS3001 In distribution
MDS3003 In distribution
MDS9133 In distribution
MDS9772 In distribution
MDS4003 In distribution
MDS3002 In distribution
MDS9136 In distribution
MDS9133 In distribution
MDS9114 In distribution
MDS9771 In distribution
MDS9119 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Baum W.A. Baum Co., Inc. 116
Alphamed Shenzhen Urion Technology Co., Ltd. 68
Electronic Blood Pressure Monitor Shenzhen Pango Electronic Co., Ltd. 59
Arm Type Automatic Blood Pressure Monitor Shenzhen Jiacom Technology Co., Ltd. 58
A&D Medical A&D Company, Ltd. 56
Diagnostix™ American Diagnostic Corp. 54
Lutech Lutech Industries 51
Veridian Veridian Healthcare 50
Hopkins Medical Products® Hopkins Uniform Company 49
Welch Allyn, Inc. Welch Allyn, Inc. 49
Merit Medical® Argon Critical Care Systems Singapore PTE. Ltd. 48
SunTech Suntech Medical, Inc. 46

Showing 12 of 1,292. All products under System, Measurement, Blood-Pressure, Non-Invasive

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K761302 1977-01-05

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Medline
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medline Industries, LP – Northfield UDI-DI 2024-08-30 Class II Under Investigation by firm It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as well as overheating at times making the unit warm to the to 52,521 units

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