All Soft Ureteral Stent - 7F, 22cm with Suture SOT 7/22-S

GUDID 10812261013210

Polymeric ureteral stent

Primary Device ID	10812261013210
NIH Device Record Key	73d3aac5-4f61-4966-abbe-4f38e25d67b7
Commercial Distribution Status	In Commercial Distribution
Brand Name	All Soft Ureteral Stent - 7F, 22cm with Suture
Version Model Number	7F, 22cm with Suture
Catalog Number	SOT 7/22-S
Company DUNS	796354509
Company Name	ALLWIN MEDICAL DEVICES, INC.
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	true
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00812261013213 [Primary]
GS1	10812261013210 [Package] Contains: 00812261013213 Package: [10 Units] In Commercial Distribution

FAD	Stent, Ureteral

Steralize Prior To Use	false
Device Is Sterile	true

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