AccessGUDID - DEVICE: INSTRUMENT (07613327319910)

GUDID

Device Identifier (DI) Information

Brand Name: INSTRUMENT
Version or Model: I-H0659HA51
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: I-H0659HA51
Company Name: Howmedica Osteonics Corp.

Primary DI Number: 07613327319910
Issuing Agency: GS1
Commercial Distribution End Date: October 02, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 058311945 *Terms of Use

Device Description: SPECIALTY TRIDENT ACETABULAR HIGH RIM REAMER

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:	No
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?
32848	Acetabular orthopaedic reamer	An orthopaedic surgical instrument designed to cut and resurface with precision the acetabulum for the acceptance of the acetabular component of a hip joint prosthesis. The device is designed with a hemispherical shell with an abrasive outer surface as the cutting head that is attached to a shaft for manual or powered rotation. It is typically made of a high-grade stainless steel alloy and is available in various sizes. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LWJ	Prosthesis, hip, semi-constrained, metal/polymer, uncemented
MAY	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish
MBL	Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous
LZO	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
KWZ	Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
KWL	Prosthesis, hip, hemi-, femoral, metal
LPH	PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
MEH	Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate
KWY	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
HWC	Screw, fixation, bone
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented

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: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Diameter: 51.0 Millimeter

Device Record Status

Public Device Record Key: f0d66410-3120-4fc1-a9c3-e428c7832336
Public Version Date: January 03, 2024
Public Version Number: 3
DI Record Publish Date: September 24, 2016