Dura-CUF

Dura-CUF, Small Adult, 2 TB Screw, 17 - 25 CM, Singledura-CUF, Small Adult, 2 TB Screw, 17 - 25 CM, Single

Registry build 21.09.26
50manufacturers in China registered for this device type
54catalogue numbers in this listing
4510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Guangdong (22), Zhejiang (13), Jiangsu (7). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DXQ
Manufacturer City Province Registered as Device types
Wenzhou Caretek Medical Device Co., Ltd. Wenzhou Zhejiang Contract manufacturer 30
Shenzhen MED-Link Electronics Tech Co., Ltd. Shenzhen Guangdong Contract manufacturer 18
Sunmed AP, Ltd. Zhuhai Guangdong Contract manufacturer 18
Sunmed AP, Ltd., Warehouse NO. 2 Zhuhai Guangdong Contract manufacturer 16
Heyuan Hong DE Medical Products Co., Ltd. Heyuan Guangdong Contract manufacturer 13
Ningbo Xinwell Medical Technology Co., Ltd. Cixi Zhejiang Contract manufacturer 12
Suzhou Minhua Medical Equipment Co., Ltd. Suzhou Jiangsu Contract manufacturer 9
A&D Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Suntech Medical Devices (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 2
Shanghai Minhua Medical Apparatus Supplies Co., Ltd. Shanghai Shanghai Contract manufacturer 1
Wenzhou Naisi Health Product Co., Ltd. Wenzhou Zhejiang Contract manufacturer 1
Huzhou Junda Industry Co., Ltd. Anji Zhejiang Contract manufacturer 129

Showing 12 of 50. All 50 manufacturers in China registered for Blood Pressure Cuff

Record

Regulatory record for Dura-CUF
Listed by GE Medical Systems Information Technologies, Inc., United States
FDA product code DXQ
Device type Blood Pressure Cuff
Device class Class 2
Regulation 21 CFR 870.1120
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K120125
Record published 2016-06-30
Record revised 2026-01-30 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, manufacturing date
Storage Storage environment temperature -20 to 55 °C; Storage environment humidity 15 to 95 % RH
Packaging Pack of 5
Distribution end date 2025-04-01

Catalogue Numbers

Catalogue numbers for Dura-CUF
Catalogue number Size Status
DUR-A3-2A Large Adult In distribution
DUR-T1-2A Thigh In distribution
2130 Adult Long In distribution
2279 Thigh In distribution
DUR-A3-2A-L Large Adult Long In distribution
DUR-A2-2A Adult In distribution
DUR-A2-2A-L Adult Long In distribution
2274 Infant In distribution
2276 Small Adult In distribution
002275 Child In distribution
2131 Large Adult Long In distribution
DUR-P2-2A Child In distribution
DUR-A1-2A-L Small Adult Long In distribution
DUR-P1-2A Infant In distribution
2278 Large Adult In distribution
DUR-P2-2A-L Child Long In distribution
DUR-A1-2A Small Adult In distribution
002277 Adult In distribution
2752 Small Adult Withdrawn
2750 Infant Withdrawn
002781 Child Withdrawn
002204 Large Adult Long Withdrawn
002764 Adult Withdrawn
002796 Thigh Withdrawn
002760 Infant Withdrawn
2754 Large Adult Withdrawn
002774 Adult Withdrawn
002791 Large Adult Withdrawn
002205 Thigh Withdrawn
002765 Adult Long Withdrawn
002766 Large Adult Withdrawn
002206 Adult Long Withdrawn
002772 Large Adult Withdrawn
002207 Large Adult Long Withdrawn
002203 Adult Withdrawn
002757 Large Adult Long Withdrawn
2785 Child Long Withdrawn
2753 Adult Withdrawn
002784 Large Adult Long Withdrawn
002783 Infant Withdrawn
002202 Small Adult Withdrawn
2755 Thigh Withdrawn
002756 Adult Long Withdrawn
002779 Small Adult Withdrawn
2751 Child Withdrawn
002767 Large Adult Long Withdrawn
002771 Adult Withdrawn
002761 Child Withdrawn
002768 Thigh Withdrawn
002769 Child Long Withdrawn
2200 Infant Withdrawn
002763 Small Adult Long Withdrawn
002762 Small Adult Withdrawn
002201 Child Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Unimed Unimed Medical Supplies Inc 1,801
Welch Allyn, Inc. Welch Allyn, Inc. 1,310
Diagnostix™ American Diagnostic Corp. 681
Orantech Orantech Inc. 648
Blood Pressure Cuff Salter Labs 425
Aneroids (82 etc.) Rashman Corp. 418
Medline Medline Industries, Inc. 390
Baum W.A. Baum Co., Inc. 349
Adcuff™ American Diagnostic Corp. 348
Disposable cuff Suntech Medical, Inc. 326
Vistarmed Shenzhen Vistar Medical Supplies Co., Ltd. 254
Statcorp Medical Statcorp, Inc. 229

Showing 12 of 598. All products under Blood Pressure Cuff

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K230145 2023-03-14
K123996 2013-04-09
K120125 2012-10-03
K022482 2002-08-13

Recalls

1 of these is 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
2024-04-09 Class II Under Investigation by firm Use of the blood pressure cuffs could result in inaccurate non-invasive blood pressure measurements. 23,180/20-cuff boxes

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