Poly-Tape 20 mm x 800 mm 102-1082

GUDID 05060267132536

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 ID05060267132536
NIH Device Record Keyda647f93-6029-4124-b148-fc11fe1d7c69
Commercial Distribution StatusIn Commercial Distribution
Brand NamePoly-Tape 20 mm x 800 mm
Version Model Number102-1082
Catalog Number102-1082
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
GS105060267132536 [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

Devices Manufactured by XIROS LTD

05060267133755 - Pitch-Patch2023-10-13 Tissue Reinforcement Device
05060267133762 - Pitch-Patch2023-10-13 Tissue Reinforcement Device
05060267133298 - Xiros 2023-08-03 6mm x 23mm Fastlok
05060267133304 - Xiros2023-08-03 8mm x 23mm Fastlok
05060267131812 - Poly-Tape2023-07-11 Poly-Tape 30mm x 800mm
05060267132697 - Rigid Probe2023-04-06
05060267132703 - Malleable Probe2023-04-06
05060267132499 - Poly-Tape 5 mm x 800 mm 2022-10-24

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