LiquiBand XL

GUDID 05036912001489

ADVANCED MEDICAL SOLUTIONS (PLYMOUTH) LIMITED

Wound closure set, topical Wound closure set, topical Wound closure set, topical Wound closure set, topical Wound closure set, topical
Primary Device ID05036912001489
NIH Device Record Key1e846bbd-7d2f-45b8-94d3-01efbd118194
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiquiBand XL
Version Model Number72014046
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
Phone+448444125754
EmailInfo@LiquiBand.com
Phone+448444125754
EmailInfo@LiquiBand.com
Phone+448444125754
EmailInfo@LiquiBand.com
Phone+448444125754
EmailInfo@LiquiBand.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105036912001472 [Primary]
GS105036912001489 [Package]
Contains: 05036912001472
Package: Carton [2 Units]
In Commercial Distribution
GS105036912001496 [Package]
Package: Shipper Carton [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OMDCutaneous Tissue Adhesive With Mesh

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-06-08
Device Publish Date2022-05-31

On-Brand Devices [LiquiBand XL]

0503691200148972014046
0503691200139772014027
0503691200124372014019
0503691200166372014046A

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