Primary Device ID | 05060267133755 |
NIH Device Record Key | 61298bfc-303f-4688-b1ba-1d164f0d7781 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pitch-Patch |
Version Model Number | 102-1090 |
Catalog Number | 102-1090 |
Company DUNS | 228209805 |
Company Name | XIROS LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk | |
Phone | +441132387202 |
enquiries@xiros.co.uk |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Length | 30 Millimeter |
Width | 20 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060267133755 [Primary] |
OWX | Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-13 |
Device Publish Date | 2023-10-05 |
05060267132024 | Tissue Reinforcement Device |
05060267132017 | Tissue Reinforcement Device |
05060267133762 | Tissue Reinforcement Device |
05060267133755 | Tissue Reinforcement Device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PITCH-PATCH 74081758 1756139 Dead/Cancelled |
Brown, Linn P., Jr. 1990-07-25 |