T-SPeC 114

GUDID 08569950031141

Suprapubic drainage catheter

Primary Device ID	08569950031141
NIH Device Record Key	7759d8ac-7e1b-4e5a-9c55-8ea547e316de
Commercial Distribution Discontinuation	2020-03-31
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	T-SPeC
Version Model Number	T14
Catalog Number	114
Company DUNS	795608012
Company Name	SWAN VALLEY MEDICAL, INCORPORATED
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	true
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
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	08569950031141 [Primary]

FEX	Instrument, Catheter, Punch

Steralize Prior To Use	false
Device Is Sterile	true

00856995003010	Transurethral Suprapubic endo-Cystostomy
00856995003003	Transurethral Suprapubic endo-Cystostomy
08569950031141	Transurethral Suprapubic endo-Cystostomy
08569950031073	Transurethral Suprapubic endo-Cystostomy

Mark Image Registration \| Serial	Company Trademark Application Date
T-SPEC 98222761 not registered Live/Pending	Swan Valley Medical, Inc. 2023-10-13
T-SPEC 88861163 not registered Live/Pending	Nissan Jidosha Kabushiki Kaisha 2020-04-06
T-SPEC 85672663 4292325 Live/Registered	Swan Valley Medical, Incorporated 2012-07-10
T-SPEC 77433197 4171930 Live/Registered	Swan Valley Medical, Incorporated 2008-03-27