Infinity-Lock 3 102-1100

GUDID 05060267132543

XIROS LTD

Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament Polyester suture, non-bioabsorbable, multifilament
Primary Device ID05060267132543
NIH Device Record Key5bf969ae-5998-4f09-bac2-18cfb0285e6e
Commercial Distribution StatusIn Commercial Distribution
Brand NameInfinity-Lock 3
Version Model Number102-1100
Catalog Number102-1100
Company DUNS228209805
Company NameXIROS LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk
Phone+441132387202
Emailenquiries@xiros.co.uk

Device Identifiers

Device Issuing AgencyDevice ID
GS105060267132543 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OWXMesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-24
Device Publish Date2022-10-14

On-Brand Devices [Infinity-Lock 3]

05060267131928Infinity-Lock 3
05060267132543102-1100

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