FDA UDI In Commercial Distribution 🇺🇸 United States

Catalyst CSR Shoulder System

DI: 00851388006739 · Model: 1226-7200-008 · CATALYST ORTHOSCIENCE INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Catalyst CSR Shoulder System
Primary DI
00851388006739
Version / Model
1226-7200-008
Company Name
CATALYST ORTHOSCIENCE INC.
Labeler DUNS
079702565
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-16
Public Version
1
Public Version Date
2018-08-16
Public Version Status
New
Public Device Record Key
0cb0d981-4422-4215-a9c1-805a18dd388d

Device Description

Humeral Implant, Size H

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
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

GMDN Terms

Code Name
48089 Resurfacing humeral head prosthesis

Identifiers

Type ID
Primary 00851388006739

Customer Contacts

Phone
800-587-5137