AccessGUDID - DEVICE: Implant Partners (M68426000025WD1)

GUDID

Device Identifier (DI) Information

Brand Name: Implant Partners
Version or Model: 26000025WD
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 26000025WD
Company Name: Microport Orthopedics Inc.

Primary DI Number: M68426000025WD1
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 079118736 *Terms of Use

Device Description: COCR SF FEM HEAD 36MM SLT TPR SHRT NK IMPLANT PARTNERS™

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?
33175	Metallic femoral head prosthesis	An implantable artificial substitute for a diseased or injured femoral head that has an outer surface made of metal [e.g., cobalt-chrome (Co-Cr), titanium (Ti), stainless steel]. It is designed to be attached to the trunnion of a prosthetic femoral stem/shaft or a head/stem adaptor, and to articulate with an acetabulum prosthesis as part of a total hip arthroplasty (THA), or articulate with the natural acetabulum directly or via a bipolar component as part of a partial hip arthroplasty (hemiarthroplasty). The device ranges in form from partially to fully spherical (ball-shaped) and is available in various sizes.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
KWA	Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
JDL	Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

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
Lumen/Inner Diameter: 36 Millimeter

Device Record Status

Public Device Record Key: 804ce1c9-223b-4ddd-b333-dc72098af6ef
Public Version Date: April 06, 2020
Public Version Number: 3
DI Record Publish Date: October 23, 2015