NA

GUDID 16959664900106

Hangzhou AGS MedTech Co., Ltd.

Gastro-urological guidewire, single-use
Primary Device ID16959664900106
NIH Device Record Key7ad856c1-611d-4f11-819f-e406270f7e08
Commercial Distribution StatusIn Commercial Distribution
Brand NameNA
Version Model NumberAG-5041-2526
Company DUNS542984702
Company NameHangzhou AGS MedTech Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106959664900109 [Primary]
GS116959664900106 [Package]
Contains: 06959664900109
Package: box [10 Units]
In Commercial Distribution
GS126959664900103 [Package]
Package: carton [100 Units]
In Commercial Distribution

FDA Product Code

OCYEndoscopic Guidewire, Gastroenterology-Urology

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-17
Device Publish Date2022-10-09

On-Brand Devices [ NA]

16959664912123AG-5099-05
16959664912055AG-5098-0525
16959664900830AG-5063-S2524G
16959664900786AG-5062-N3024G
16959664900779AG-5062-N2524G
16959664900762AG-5062-N2024G
16959664900106AG-5041-2526
16959664900021AG-5041-3526
16959664900014AG-5041-2526

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