iTind Removal Kit

GUDID 07290015518192

Bare-metal urethral stent, short-term

Primary Device ID	07290015518192
NIH Device Record Key	d060eec4-b401-4abd-89b6-1aea18d56567
Commercial Distribution Status	In Commercial Distribution
Brand Name	iTind Removal Kit
Version Model Number	MT-FA08
Company DUNS	532003626
Company Name	MEDI-TATE LTD
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
Human Cell/Tissue Product	false
Device Kit	false
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	07290015518192 [Primary]

QKA	Temporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia

Steralize Prior To Use	false
Device Is Sterile	true

07290015518192 - iTind Removal Kit	2023-11-02iTind Removal Kit: 1 Snare + 1 Removal Tube
07290015518192 - iTind Removal Kit	2023-11-02 iTind Removal Kit: 1 Snare + 1 Removal Tube
07290015518062 - iTIND System	2023-07-25 iTIND System
07290015518079 - iTIND	2023-07-25
07290015518086 - SNARE	2023-07-25
07290015518109 - iTIND System	2023-07-25 iTIND System Box of 5
17290015518083 - Snare X5	2021-07-28 Pack of 5 individually packed Snare