Align® TO Trans-Obturator Urethral Support System - Hook & Halo BRD600HH

GUDID 00801741016233

ALIGN® TO Urethral Support System, Hook & Halo

C. R. Bard, Inc.

Stress urinary incontinence surgical mesh, female
Primary Device ID00801741016233
NIH Device Record Key662406a3-142a-42c3-967b-5501fb9c2234
Commercial Distribution Discontinuation2016-12-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameAlign® TO Trans-Obturator Urethral Support System - Hook & Halo
Version Model NumberBRD600HH
Catalog NumberBRD600HH
Company DUNS016898496
Company NameC. R. Bard, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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

Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741016233 [Primary]
GS110801741016230 [Package]
Package: Other [1 Units]
Discontinued: 2016-12-31
Not in Commercial Distribution

FDA Product Code

OTNmesh, surgical, synthetic, urogynecologic, for stress urinary incontinence, retropubic or transobturator

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-04-23
Device Publish Date2015-09-14

Devices Manufactured by C. R. Bard, Inc.

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10801741226981 - PureWick2024-08-06 PureWick Flex Female External Catheter, Home Care
10801741226462 - PureWick2024-06-10 PureWick Male External Catheter, Home Care
10801741226950 - PureWick2024-06-10 PureWick Flex Female External Catheter Kit
10801741218788 - SureStep Foley Tray System2024-05-21 SureStep Foley Tray Kit optimized for Sensica UO System
10801741218832 - SureStep Foley Tray System2024-05-21 SureStep Foley Tray Kit optimized for Sensica UO System
10801741171663 - Bardia2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
20801741171677 - Bardia2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter

Trademark Results [Align]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ALIGN
ALIGN
98525294 not registered Live/Pending
Portals Paper Limited
2024-04-29
ALIGN
ALIGN
98474424 not registered Live/Pending
GILMAN BROTHERS COMPANY, THE
2024-03-29
ALIGN
ALIGN
98449553 not registered Live/Pending
BenDavid, Dina
2024-03-14
ALIGN
ALIGN
98376430 not registered Live/Pending
Civco Medical Instruments Co., Inc.
2024-01-25
ALIGN
ALIGN
97826844 not registered Live/Pending
Tidal Vision Products, Inc.
2023-03-07
ALIGN
ALIGN
97826830 not registered Live/Pending
Tidal Vision Products, Inc.
2023-03-07
ALIGN
ALIGN
97796036 not registered Live/Pending
BenDavid, Dina
2023-02-15
ALIGN
ALIGN
97730584 not registered Live/Pending
Self-Help Technologies
2022-12-23
ALIGN
ALIGN
97616631 not registered Live/Pending
IntelliGenesis, LLC
2022-10-03
ALIGN
ALIGN
97469934 not registered Live/Pending
American Sentinel University, Inc.
2022-06-22
ALIGN
ALIGN
97467644 not registered Live/Pending
BBFIT STUDIO PTY LTD
2022-06-21
ALIGN
ALIGN
97420705 not registered Live/Pending
ALIGN SOFTWARE CORPORATION
2022-05-20

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