FDA UDI In Commercial Distribution 🇺🇸 United States

HUMERIS 135

DI: 03701037310397 · Model: 322-0609 · FX SOLUTIONS
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HUMERIS 135
Primary DI
03701037310397
Version / Model
322-0609
Catalog Number
322-0609
Company Name
FX SOLUTIONS
Labeler DUNS
263076196
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-11
Public Version
1
Public Version Date
2023-01-19
Public Version Status
New
Public Device Record Key
cb8c86f8-e16f-4c84-8a5d-0f65e2907769

Device Description

HUMERAL CUP ECCENTRIC SYMMETRIC MOBILITY PE/TA6V Ø32+9 / TAPER Ø10

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PHX Shoulder Prosthesis, Reverse Configuration
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

GMDN Terms

Code Name
48092 Polyethylene reverse shoulder prosthesis cup

Identifiers

Type ID
Primary 03701037310397

Premarket Submissions

Submission Number Supplement Number
K222936 000