AccessGUDID - DEVICE: G7 BALL HEX DRIVER FOR INSERTER (00880304926820)

GUDID

Device Identifier (DI) Information

Brand Name: G7 BALL HEX DRIVER FOR INSERTER
Version or Model: 010002736
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 010002736
Company Name: Biomet Orthopedics, LLC

Primary DI Number: 00880304926820
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:	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?
32871	Surgical torque wrench, reusable	A hand-held manual surgical instrument intended to be used for gripping, turning/tightening, or twisting an object (e.g., a nut, bolt, or wire) during a surgical intervention; it is not dedicated to dental use only. It may be available in a variety of forms and might have fixed or adjustable jaws, or a detachable endpiece(s) [e.g., ratchet type]. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KWZ	Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
PBI	prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented
OQG	Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
OQI	Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
LPH	PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
OQH	Hip, semi-constrained, cemented, metal/polymer + additive, cemented
LZO	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
LWZ	TISSUE GRAFT OF LESS THAN 6MM

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K121874	000

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
No Device Sizes

Device Record Status

Public Device Record Key: 820960af-06fb-4595-a0c5-7f70321bfc90
Public Version Date: May 30, 2025
Public Version Number: 7
DI Record Publish Date: September 23, 2016