LiquiBand Octyl

GUDID 05036912001090

ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

Skin-approximation adhesive
Primary Device ID05036912001090
NIH Device Record Keybcf0c45b-c501-46a0-92b2-4c132e6ca05b
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiquiBand Octyl
Version Model Number72014016
Company DUNS236059171
Company NameADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED
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

Phone+448444125754
EmailInfo@LiquiBand.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105036912001045 [Primary]
GS105036912001076 [Package]
Contains: 05036912001045
Package: Carton [10 Units]
In Commercial Distribution
GS105036912001090 [Package]
Contains: 05036912001076
Package: Shipper Carton [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MPNTissue Adhesive For The Topical Approximation Of Skin

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-06

Devices Manufactured by ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

05036912001595 - INTEGUSEAL2024-12-04 IS100
05036912001625 - INTEGUSEAL2024-12-04 IS200
05036912001427 - LIQUIFIX FIX82023-07-03
05036912001458 - LIQUIFIX Precision Open2023-07-03
05036912000406 - LiquiBand Butyl2023-06-20
05036912001694 - LiquiBand Exceed2023-06-20
05036912001724 - LiquiBand Exceed XS2023-06-20
05036912001755 - LiquiBand Octyl Mini2023-06-20

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