AccessGUDID - DEVICE: S³PROXIMAL HUMERUS PLATE 11 HOLE LEFT (00887868072956)

GUDID

Device Identifier (DI) Information

Brand Name: S³PROXIMAL HUMERUS PLATE 11 HOLE LEFT
Version or Model: SSPL11
Commercial Distribution Status: In Commercial Distribution
Catalog Number: SSPL11
Company Name: Biomet Orthopedics, LLC

Primary DI Number: 00887868072956
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?
46647	Orthopaedic fixation plate, non-bioabsorbable	A non-bioabsorbable, non-customized, firm, implantable sheet intended to stabilize a fractured orthopaedic bone (excluding craniofacial and spinal) to treat a traumatic/pathological fracture, to fuse a joint (arthrodesis) and/or as part of an osteotomy. Typically attached to a bone of a limb, rib, sternum, or pelvis, it is designed to be fixed in place with screws, and may be used in connection with another fixation plate; it does not incorporate a sleeve or blade. Instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be included with the plate.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HRS	PLATE, FIXATION, BONE
JDW	PIN, FIXATION, THREADED
KTT	APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
HTY	PIN, FIXATION, SMOOTH
HWC	Screw, fixation, bone
HSB	ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
HTN	WASHER, BOLT NUT
LXT	APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

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: 11 HOLE LEFT

Device Record Status

Public Device Record Key: 665c3c60-7f52-4717-988d-78e6e8f6122d
Public Version Date: May 30, 2025
Public Version Number: 7
DI Record Publish Date: October 24, 2015