DLP®

Adapter 14031 Mult Perf SET Vent 10P 17L

Registry build 21.09.26
13manufacturers in China registered for this device type
51catalogue numbers in this listing
3510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (3), Beijing (3), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DTL
Manufacturer City Province Registered as Device types
Shanghai INT Medical Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 10
Elite Medtek(Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 9
Tianjin Demax Medical Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 5
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Zhejiang Mediunion Healthcare Group Co., Ltd. Ningbo Zhejiang Contract manufacturer 105
Joykey Industrial (Pinghu) Limited Pinghu Zhejiang Contract manufacturer 43
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Tianck Medical Co., Ltd. Huizhou Guangdong Manufacturer 10
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
Beijing Demax Medical Technology Co., Ltd. Beijing Beijing Manufacturer 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5

Showing 12 of 13. All 13 manufacturers in China registered for Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

Record

Regulatory record for DLP®
Listed by Medtronic, Inc., United States
FDA product code DTL
Device type Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device class Class 2
Regulation 21 CFR 870.4290
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K790563
Record published 2016-05-22
Record revised 2025-03-03 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number
Storage Storage environment temperature up to 40 °C
Sizes Length 0.64 to 50.8 cm; outer diameter 0.64 cm
Distribution end date 2026-01-30

Catalogue Numbers

Catalogue numbers for DLP®
Catalogue number Size Per pack Status
14013 Length 30.5 cm 10 In distribution
10022 Length 8.3 cm 40 In distribution
11001 Length 25.4 cm 10 In distribution
14031 Length 38.1 cm 10 In distribution
14003 Length 30.5 cm 10 In distribution
10004D 20 In distribution
10004 20 In distribution
10007 Length 0.64 cm 40 In distribution
10003 20 In distribution
14017 Length 38.1 cm 10 In distribution
CB10005 Length 19.1 cm In distribution
14006 Length 38.1 cm 10 In distribution
14000 Length 38.1 cm 10 In distribution
CB14017 Length 38.1 cm In distribution
9810064 10 In distribution
10710 20 In distribution
10005BH 20 In distribution
10005OS 20 In distribution
10003 20 In distribution
13003 5 In distribution
14001 Length 38.1 cm 10 In distribution
10001 Length 12.7 cm 20 In distribution
10700 20 In distribution
10005 20 In distribution
10001K Length 12.7 cm 20 In distribution
10706 20 In distribution
13001 10 In distribution
11001G Length 50.8 cm 20 In distribution
10534 20 In distribution
10001 Length 12.7 cm 20 In distribution
10001 Length 12.7 cm 20 In distribution
10008 Length 0.95 cm 40 In distribution
10001K Length 12.7 cm 20 In distribution
10005S 10 Withdrawn
65000 240 mmHg 10 Withdrawn
14014 Length 30.5 cm 10 Withdrawn
14016 Length 38.1 cm 10 Withdrawn
10004C 20 Withdrawn
10535 20 Withdrawn
CB10005 Withdrawn
CB10007 Length 0.64 cm Withdrawn
13002 20 Withdrawn
10704 10 Withdrawn
10003OS 20 Withdrawn
10003S 20 Withdrawn
10533 20 Withdrawn
14002 Length 30.5 cm 20 Withdrawn
10003OS 20 Withdrawn
65125 125 mmHg 10 Withdrawn
CB14017 Withdrawn
CB10004 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeRoyal Deroyal Industries, Inc. 171
Namic Medline Industries, Inc. 170
Namic Navilyst Medical, Inc. 165
Merit® Manifold Merit Medical Systems, Inc. 119
Connector LivaNova USA, Inc. 70
Medline Industries, Inc. Medline Industries, Inc. 62
Demax Beijing Demax Medical Technology Co., Ltd. 60
Marquis® Stopcock Merit Medical Systems, Inc. 40
Cook Cook Incorporated 38
Unbranded Advance Medical Designs, Inc. 30
Contrast Line Argon Medical Devices, Inc. 25
INT Shanghai Kindly Medical Instruments Co., Ltd. 18

Showing 12 of 127. All products under Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K123448 2012-12-13
K122811 2012-10-12
K113845 2012-01-25

Recalls Naming This Product

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

Recalls naming the identifiers of DLP®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medtronic Perfusion Systems UDI-DI 2024-03-19 Class II Process control Potential for unsealed sterile packing. 6290 units

Recalls

The FDA has not published a severity grade for these. 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
2008-08-27 Not classified Process control Medtronic has identified an issue with the packaging for specific lots of the Medtronic Adjustable Valve and valves contained in the Attain Left Heart Delivery System kits. A small number of valve package seals could be compromised. 35,193 total 2011-05-07

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