Outlook®

Outlook® Pump Measured Volume Solution Administration Set with SAFELINE® Injection Sites, w/o Auto Shut Off

Registry build 21.09.26
49manufacturers in China registered for this device type
49catalogue numbers in this listing
22510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Zhejiang (12), Jiangsu (11), Shanghai (10). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FPA
Manufacturer City Province Registered as Device types
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Hantech Medical Device Co., Ltd. Cixi Zhejiang Contract manufacturer 18
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14
BQ Plus Medical Co., Ltd. Songjiang Shanghai Contract manufacturer 13
Ningbo Tianyi Medical Appliance Co., Ltd. Ningbo Zhejiang Contract manufacturer 11
Anhui Tiankang Medical Technology Co., Ltd. Tianchang Anhui Contract manufacturer 9
Anhui Kangda Medical Products Co., Ltd. Tianchang Anhui Contract manufacturer 7
JDI Electronics Factory Dongguan Guangdong Contract manufacturer 7
Yangzhou Xingwei Medical Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 5
Wenzhou K.L.F. Medical Plastics Co., Ltd. Wenzhou Zhejiang Contract manufacturer 4
Advance Technology Ltd Shenzhen Guangdong Contract manufacturer 3
Weihai Jierui Medical Products Co., Ltd. Weihai Shandong Contract manufacturer 3

Showing 12 of 49. All 49 manufacturers in China registered for Set, Administration, Intravascular

Record

Regulatory record for Outlook®
Listed by B. Braun Medical Inc., United States
FDA product code FPA
Device type Set, Administration, Intravascular
Device class Class 2
Regulation 21 CFR 880.5440
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2016-09-23
Record revised 2023-02-17 (version 8)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Distribution end date 2022-08-27

Catalogue Numbers

Catalogue numbers for Outlook®
Catalogue number Size Per pack Status
354213 24 In distribution
354212 24 In distribution
352034 24 In distribution
352425 24 In distribution
V7410 24 In distribution
375511 20 In distribution
470178 24 In distribution
352520 24 In distribution
352458 24 In distribution
375038 20 In distribution
470025 50 In distribution
354216 24 In distribution
375122 20 In distribution
474004 24 In distribution
352461 24 In distribution
375118 20 In distribution
US3130 24 In distribution
470024 50 In distribution
352430 24 In distribution
354215 20 In distribution
V7405 24 In distribution
375512 20 In distribution
NF3140-10 24 In distribution
NF3106 24 In distribution
NF3191 24 In distribution
US3120 24 In distribution
352033 24 In distribution
NF3140 24 In distribution
V7450 24 In distribution
375150 20 In distribution
NF3120 24 In distribution
470018 24 In distribution
352472 24 In distribution
US3181 24 In distribution
470177 24 In distribution
354214 24 In distribution
V7400 24 In distribution
352475 24 In distribution
V7453 24 In distribution
V7490 24 In distribution
470019 24 In distribution
490074 24 Withdrawn
375196 24 Withdrawn
SS3140 24 Withdrawn
US3180 24 Withdrawn
470046 24 Withdrawn
352442 24 Withdrawn
474001 24 Withdrawn
375040 20 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ICU Medical ICU Medical, Inc 529
Codan Codan US Corp. 510
Vygon Vygon Corp. 355
Port Access Needle Bard Access Systems, Inc. 341
Set, Administration, Intravascular Mps Medical, Inc. 291
Alaris, SmartSite BD Switzerland Sàrl 266
IV Administration Set B. Braun Medical Inc. 242
Medex ICU Medical, Inc 237
Extension Set B. Braun Medical Inc. 171
MaxGuard BD Switzerland Sàrl 150
Medline Medline Industries, Inc. 148
Centurion Centurion Medical Products Corporation 145

Showing 12 of 768. All products under Set, Administration, Intravascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243392 2025-07-24
K213778 2022-03-03
K212842 2022-01-18
K202618 2021-09-24
K191658 2020-03-19
K173361 2018-06-26
K170595 2017-11-07
K153293 2016-04-06
K143082 2015-07-24
K140838 2014-12-05
K142036 2014-08-25
K140311 2014-05-07
K112636 2011-11-26
K083723 2009-06-05
K073396 2008-08-07
K052252 2005-11-16
K041490 2004-10-29
K031923 2003-08-11
K021488 2002-07-08
K974145 1998-01-06
K955585 1996-05-15
K954123 1995-11-21

Recalls Naming This Product

5 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Outlook®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
B. Braun Medical Inc. UDI-DI 2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 18,072 untis
B. Braun Medical Inc. UDI-DI 2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 162,648 untis
B. Braun Medical Inc. UDI-DI 2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 0
B. Braun US Device Manufacturing LLC UDI-DI 2024-06-17 Class II Process control Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and 236208 units
B. Braun US Device Manufacturing LLC UDI-DI 2024-06-17 Class II Process control Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and 88968 units

Recalls

38 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
2026-08-04 Class II Under Investigation by firm Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. 25850
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 11,832 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 27,480 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 19,320 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 12,320 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 13,600 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 65,904 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 12,700 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 18,984 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 1,861,111 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 960 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 80,650 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 6,768 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 48,672 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 100 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 66,792 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 29,900 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 259,392 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 286,400 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 164,568 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 40,992 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 74,652 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 19,392 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 5,448 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 11,650 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 381,850 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 43,452 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 49,330,370
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 554,015 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 190,625 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 37,656 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 88,200 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 6,672 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 30,250 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 98,568 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 28,344 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 41,400 units
2025-10-29 Class II Process control Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). 19,104 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