16959664932442 Medical Device Identification

GUDID 16959664932442

General-purpose endoscopic needle, single-use

Primary Device ID	16959664932442
NIH Device Record Key	53fd2f09-d4e5-4406-83f2-9e7274277094
Commercial Distribution Status	In Commercial Distribution
Version Model Number	AG-5311-2423-2404
Company DUNS	542984702
Company Name	Hangzhou AGS MedTech Co., Ltd.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	06959664932445 [Primary]
GS1	16959664932442 [Package] Contains: 06959664932445 Package: Box [10 Units] In Commercial Distribution
GS1	26959664932449 [Package] Package: Carton [100 Units] In Commercial Distribution

FBK	Endoscopic Injection Needle, Gastroenterology-Urology

Steralize Prior To Use	false
Device Is Sterile	true