Resp-O2 Disposable Guedel Airway, 110 Mm, Adult X-Large, Orange

Catalogue number 36322, listed by Dynarex Corp., United States, under Airway, Oropharyngeal, Anesthesiology. 84 manufacturers in China are registered for this product code.

Registry build 21.09.26
84manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Zhejiang (30), Guangdong (18), Jiangsu (12). 20 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CAE
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Guangzhou Nuoning Medical Supplies Co., Ltd. Guangzhou Guangdong Contract manufacturer 62
Gcmedica Enterprise Ltd.(Wuxi) Wuxi Jiangsu Contract manufacturer 55
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Ningbo Luke Medical Devices Co., Ltd. Yuyao Zhejiang Contract manufacturer 27
Zhejiang Haisheng Medical Device Co., Ltd. Shaoxing Zhejiang Contract manufacturer 21
Tylenol Medical Instruments Co., Ltd. Zhongshan Guangdong Contract manufacturer 15
IPE Plastic & Hardware Industy, Ltd Dongguan Guangdong Contract manufacturer 15
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14
Ningbo Great Mountain Medical Instruments Co., Ltd. Ningbo Zhejiang Contract manufacturer 12

Showing 12 of 84. All 84 manufacturers in China registered for Airway, Oropharyngeal, Anesthesiology

Record

Regulatory record for Resp-O2 Disposable Guedel Airway, 110 mm, Adult X-Large, Orange
Listed by Dynarex Corp., United States
FDA product code CAE
Device type Airway, Oropharyngeal, Anesthesiology
Device class Class 1
Regulation 21 CFR 868.5110
Establishment Specification developer, Manufacturer
Premarket notification Exempt
Record published 2024-12-20

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Packaging Box of 10, shipper of 50

Catalogue Numbers

Catalogue numbers for Resp-O2 Disposable Guedel Airway, 110 mm, Adult X-Large, Orange
Catalogue number Size Status
36322 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LMA Airway Management Teleflex Medical LLC 444
Rusch Teleflex Medical LLC 129
SourceMark Sourcemark, LLC. 94
Curaplex Bound Tree Medical, LLC 86
Hudson RCI Teleflex Medical LLC 83
SunMed SunMed Group Holdings, LLC 66
Medline Medline Industries, Inc. 59
LMA Teleflex Medical LLC 50
MediChoice Owens & Minor Distribution, Inc. 33
ADC® American Diagnostic Corp. 32
Air-Q3® Airlife, Inc. 32
Compower Xiamen Compower Medical Tech. Co., Ltd. 29

Showing 12 of 347. All products under Airway, Oropharyngeal, Anesthesiology

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K891586 1989-05-11

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