Forté® HD Access Sheath

GUDID 10607915113329

Ureteral Stent Placement Set

APPLIED MEDICAL RESOURCES CORPORATION

Ureteral stent-placement set Ureteral stent-placement set Ureteral stent-placement set
Primary Device ID10607915113329
NIH Device Record Key90f0ff14-da4c-4e8d-a7cd-9ae9891e3284
Commercial Distribution StatusIn Commercial Distribution
Brand NameForté® HD Access Sheath
Version Model NumberB7167
Company DUNS187129135
Company NameAPPLIED MEDICAL RESOURCES CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Length20 Centimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915113322 [Primary]
GS110607915113329 [Package]
Contains: 00607915113322
Package: [6 Units]
In Commercial Distribution

FDA Product Code

FEDEndoscopic Access Overtube, Gastroenterology-Urology

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-08-22

On-Brand Devices [Forté® HD Access Sheath]

10607915113565Ureteral Dilating Catheter
10607915113541Ureteral Dilating Catheter
10607915113527Ureteral Dilating Catheter
10607915113503Ureteral Dilating Catheter
10607915113381Ureteral Dilating Catheter
10607915113343Ureteral Dilating Catheter
10607915113329Ureteral Stent Placement Set
10607915113282Ureteral Stent Placement Set
10607915113268Ureteral Stent Placement Set
10607915113213Ureteral Stent Placement Set
10607915113190Ureteral Stent Placement Set
10607915113176Ureteral Stent Placement Set
10607915113152Ureteral Stent Placement Set

Trademark Results [Forté]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FORTE
FORTE
98242140 not registered Live/Pending
LivaNova USA, Inc.
2023-10-26
FORTE
FORTE
98176548 not registered Live/Pending
Jonathan Oliveira
2023-09-12
FORTE
FORTE
98074061 not registered Live/Pending
Meros America Inc
2023-07-06
FORTE
FORTE
98029782 not registered Live/Pending
FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION
2023-06-06
FORTE
FORTE
98029706 not registered Live/Pending
FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION
2023-06-06
FORTE
FORTE
98029571 not registered Live/Pending
FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION
2023-06-06
FORTE
FORTE
97773116 not registered Live/Pending
Corsa Holdings, LLC
2023-01-30
FORTE
FORTE
97773072 not registered Live/Pending
Corsa Holdings, LLC
2023-01-30
FORTE
FORTE
97674191 not registered Live/Pending
DAE DO INC
2022-11-11
FORTE
FORTE
97618722 not registered Live/Pending
ELANCO TIERGESUNDHEIT AG
2022-10-04
FORTE
FORTE
97585963 not registered Live/Pending
Forte Labs, Inc.
2022-09-09
FORTE
FORTE
97546929 not registered Live/Pending
Forte Labs, Inc.
2022-08-12

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.