HarmonyAIR

Auto Active Device, Steris

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (1), Shandong (1), Guangdong (1).

Chinese manufacturers registered for FDA product code FYD
Manufacturer City Province Registered as Device types
Zhejiang Shuyou Surgical Instrument Co., Ltd. Huzhou Zhejiang Contract manufacturer 13
BIO Protech Yantai Inc Yantai Shandong Manufacturer 12
Wickimed (Huizhou) Medical Equipment Manufacturing Co., Ltd. Huizhou Guangdong Contract manufacturer 3

Record

Regulatory record for HarmonyAIR
Listed by ConMed Corporation, United States
FDA product code FYD
Device type Apparatus, Exhaust, Surgical
Device class Class 2
Regulation 21 CFR 878.5070
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K930041
Record published 2020-09-11
Record revised 2022-11-07 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, manufacturing date
Storage Storage environment temperature 40 to 104 °F; Storage environment temperature 4 to 40 °C
Packaging Box of 2

Catalogue Numbers

Catalogue numbers for HarmonyAIR
Catalogue number Size Per pack Status
QS0028 In distribution
QS0022 2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Microtek Microtek Medical LLC 57
Surgimedics® Coastal Life Technologies, Inc. 23
Virosafe ConMed Corporation 22
Buffalo Filter Buffalo Filter Co., Inc. 22
ACU-Evac Acuderm, Inc. 21
Neptune Stryker GmbH 14
RapidVac Covidien LP 12
Megadyne Megadyne Medical Products, Inc. 12
Geiger Smoke Evacuator Filter Dermatologic LAB AND Supply, Inc. 12
Apparatus, Exhaust, Surgical Stryker GmbH 11
Apparatus, Exhaust, Surgical ConMed Corporation 10
Conmed Buffalo Filter ConMed Corporation 10

Showing 12 of 142. All products under Apparatus, Exhaust, Surgical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240127 2024-08-05
K091139 2009-05-05

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