AccessGUDID - DEVICE: G7 Freedom Acetabular Liner (00880304544574)

GUDID

Device Identifier (DI) Information

Brand Name: G7 Freedom Acetabular Liner
Version or Model: 110010282
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 110010282
Company Name: Biomet Orthopedics, LLC

Primary DI Number: 00880304544574
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 129278169 *Terms of Use

Device Description: No description.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44362	Constrained polyethylene acetabular liner	A sterile, implantable component of a two-piece acetabulum prosthesis that is inserted into an acetabular shell prosthesis to provide the articulating surface with a femoral head prosthesis as part of a total hip arthroplasty (THA). It is made of polyethylene (includes hylamer, cross-linked polyethylene) and may include a stabilizing component (e.g., a ring) to limit the range of motion of the hip to help prevent dislocation.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
LPH	PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
KWZ	Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
OQG	Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
OQH	Hip, semi-constrained, cemented, metal/polymer + additive, cemented
OQI	Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
LZO	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented
PBI	prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 36MM SHELL SIZE E LINER SIZE

Device Record Status

Public Device Record Key: 14666d77-48a9-44fa-857a-b65dfe336656
Public Version Date: May 30, 2025
Public Version Number: 5
DI Record Publish Date: November 02, 2015