Hu-Friedy

Syringe Anesthetic Aspir CW Style 1.8ml

Registry build 21.09.26
3manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

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

Chinese manufacturers registered for FDA product code EJI
Manufacturer City Province Registered as Device types
Wuxi Lyusmile IMP AND EXP Co., Ltd. Wuxi Jiangsu Private-label distributor 66
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25
Foshan Coxo Medical Instrument Co., Ltd. Foshan Guangdong Manufacturer 19

Record

Regulatory record for Hu-Friedy
Listed by HU-Friedy MFG Co., LLC, United States
FDA product code EJI
Device type Syringe, Cartridge
Device class Class 2
Regulation 21 CFR 872.6770
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2017-05-30
Record revised 2018-11-22 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Hu-Friedy
Catalogue number Size Status
SYRA In distribution
SYRCWA18 In distribution
SYRCWA22 In distribution
SYRCW In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Septodont A. Titan Instruments, Inc. 51
A. Titan Instruments A. Titan Instruments, Inc. 46
Integra® Miltex® Integra LifeSciences Production Corporation 36
Astek Young Innovations Inc. 34
Artman Instruments Wise Linkers LLC 16
Osung MND Osung MND Co., Ltd. 11
Safety Wand Handpiece Milestone Scientific, Inc. 8
Henke-Dent 500 Soft-Grip Henke-Sass Wolf, Gmbh. 8
the Wand STA Handpiece Milestone Scientific, Inc. 8
the Wand Handpiece Milestone Scientific, Inc. 8
Saftey Wand STA Handpiece Milestone Scientific, Inc. 7
J&J Instruments J & J Instruments, LLC 6

Showing 12 of 88. All products under Syringe, Cartridge

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K120659 2012-11-06

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