RIGIDLOOP 232480

GUDID 03760304680175

Tendon/ligament bone anchor, non-bioabsorbable

Primary Device ID	03760304680175
NIH Device Record Key	8568297b-0c3a-4862-8913-4cdb7fbe8580
Commercial Distribution Status	In Commercial Distribution
Brand Name	RIGIDLOOP
Version Model Number	T Adjustable Cortical System - Standard
Catalog Number	232480
Company DUNS	772462123
Company Name	S.B.M
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
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

Device Issuing Agency	Device ID
GS1	03760304680175 [Primary]

MBI	Fastener, Fixation, Nondegradable, Soft Tissue

Steralize Prior To Use	false
Device Is Sterile	true

03760304680236	The RIGIDLOOP device consists of an adjustable nonabsorbable braided loop. The implant is suppli
03760304680229	The RIGIDLOOP device consists of an adjustable nonabsorbable braided loop and titanium button, p
03760304680212	The RIGIDLOOP device consists of an adjustable nonabsorbable braided loop and titanium button, p
03760304680205	The RIGIDLOOP device consists of a titanium button, designed to be used for ACL reconstruction.
03760304680199	The RIGIDLOOP device consists of a titanium button, designed to be used for ACL reconstruction.
03760304680182	The RIGIDLOOP device consists of an adjustable nonabsorbable braided loop and titanium button, p
03760304680175	The RIGIDLOOP device consists of an adjustable nonabsorbable braided loop and titanium button, p

Mark Image Registration \| Serial	Company Trademark Application Date
RIGIDLOOP 98775049 not registered Live/Pending	Johnson & Johnson 2024-09-27
RIGIDLOOP 85803563 4656789 Live/Registered	Johnson & Johnson 2012-12-14