Dryswab

Dryswab, fine tip plastic, peel pouch rayon bud

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Jiangsu (1), Guangdong (1).

Chinese manufacturers registered for FDA product code KCL
Manufacturer City Province Registered as Device types
Yearstar Healthcare Technology Co., Ltd. Jiangyin Jiangsu Contract manufacturer 43
Huizhou Kaiyi Technology Co., Ltd. Huizhou Guangdong Manufacturer 3

Record

Regulatory record for Dryswab
Listed by Medical Wire & Equipment Company (Bath), Ltd., United Kingdom
FDA product code KCL
Device type Blower, Powder, Ent
Device class Class 1
Regulation 21 CFR 874.5220
Premarket notification Exempt
Record published 2023-10-05

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 5 to 25 °C
Packaging Box of 5000

Catalogue Numbers

Catalogue numbers for Dryswab
Catalogue number Size Per pack Status
N/a 125 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Blower, Powder, Ent Karl Storz GmbH & Co. KG 16
BR Surgical, LLC BR Surgical LLC 3
Sheehy-House Powder Insufflator Oto Med Inc 1
Kabierske Powder Blower Cannula Sontec Instruments, Inc. 1
Kabierske Powder Blower SET Sontec Instruments, Inc. 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