FDA UDI In Commercial Distribution 🇺🇸 United States

PRCT2

DI: 03701037303405 · Model: 926-1022 · FX SOLUTIONS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRCT2
Primary DI
03701037303405
Version / Model
926-1022
Catalog Number
926-1022
Company Name
FX SOLUTIONS
Labeler DUNS
263076196
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-06
Public Version
4
Public Version Date
2021-10-07
Public Version Status
Update
Public Device Record Key
0a5120c0-3c61-4bd2-b3d8-6f11c5168830

Device Description

HUMELOCK INSTRUMENT HUMELOCK TRIAL OFFSET MODULAR SYSTEM SIZE 3

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 03701037303405

Premarket Submissions

Submission Number Supplement Number
K143721 000