Portex

45 catalogue numbers from 8518, listed by ICU Medical, Inc, United States, under Resuscitator, Manual, Non Self-Inflating. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
45catalogue numbers in this listing

Who Else Makes It

Concentrated in Fujian (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NHK
Manufacturer City Province Registered as Device types
Sunmed AP, Ltd. Zhuhai Guangdong Contract manufacturer 18
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33

Record

Regulatory record for Portex
Listed by ICU Medical, Inc, United States
FDA product code NHK
Device type Resuscitator, Manual, Non Self-Inflating
Device class Class 2
Regulation 21 CFR 868.5905
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K014115
Record published 2015-09-01
Record revised 2025-04-23 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date
Packaging Box of 20, box of 15, box of 40, box of 25

Catalogue Numbers

Catalogue numbers for Portex
Catalogue number Size Status
8518 In distribution
H1008 In distribution
008440 In distribution
008235 In distribution
008432 In distribution
008435DM In distribution
008245 In distribution
008030 In distribution
008031 In distribution
385000 In distribution
008131 In distribution
008045 In distribution
008232 In distribution
008335DM In distribution
H1055 In distribution
H1041 In distribution
H1051 In distribution
008345 In distribution
008330T In distribution
H1020 In distribution
008330 In distribution
008035 In distribution
008132 In distribution
008435 In distribution
008032 In distribution
008040 In distribution
008330DM In distribution
008240 In distribution
H1054 In distribution
008230 In distribution
008430M In distribution
008330VM In distribution
385100 In distribution
008431T In distribution
008231 In distribution
008432T In distribution
008430DM In distribution
H1057 In distribution
008430T In distribution
008340 In distribution
008332DM In distribution
H1056 In distribution
008432DM In distribution
008430VM In distribution
H1025A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ventlab Ventlab, LLC 129
Hyperinflation System Mercury Medical Enterprises, LLC 64
NuFLO2 Hyperinflation System Mercury Medical Enterprises, LLC 44
Venti.Plus Galemed Corp. 6
Venti.Plus GaleMed (Xiamen) Co., Ltd. 4
Breathing Bag Mercury Medical Enterprises, LLC 4
Endure Industries Endure Industries, Inc. 2
Disposable Medical Hyperinflation System SunMed Group Holdings, LLC 2
Curaplex Bound Tree Medical, LLC 1
Ventlab Hyperinflation System Ventlab, LLC 1
Hyperinflation Mercury Medical Enterprises, LLC 1

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