MaxBlend2, 0-70 LPM High Flow for Lowenstein

Catalogue number R229P11-004, listed by Maxtec, LLC, United States, under Mixer, Breathing Gases, Anesthesia Inhalation. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code BZR
Manufacturer City Province Registered as Device types
Sunmed AP, Ltd. Zhuhai Guangdong Contract manufacturer 18
Gentec (Shanghai) Corporation Shanghai Shanghai Manufacturer 12

Record

Regulatory record for MaxBlend2, 0-70 LPM High Flow for Lowenstein
Listed by Maxtec, LLC, United States
FDA product code BZR
Device type Mixer, Breathing Gases, Anesthesia Inhalation
Device class Class 2
Regulation 21 CFR 868.5330
510(k) K161718
Record published 2018-09-18

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries serial number

Catalogue Numbers

Catalogue numbers for MaxBlend2, 0-70 LPM High Flow for Lowenstein
Catalogue number Size Status
R229P11-004 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sechrist Industries, Inc. Sechrist Industries, Inc. 43
Hyperinflation Westmed, Inc. 21
Blender Carefusion 19
Hyperinflation (Ambu) Westmed, Inc. 19
MAXBLEND2 Maxtec, LLC 17
Blender Vyaire Medical, Inc. 17
Ambu Hyperinflation System Westmed, Inc. 12
Ambu SunMed Group Holdings, LLC 12
MaxFlo2 Maxtec, LLC 11
MicroMax Maxtec, LLC 9
Bird™ Vyaire Medical, Inc. 8
Gentec® Gentec (Shanghai) Corporation 8

Showing 12 of 118. All products under Mixer, Breathing Gases, Anesthesia Inhalation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231895 2023-12-04
K161718 2016-10-27
K113232 2012-03-01

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