FDA UDI Not in Commercial Distribution 🇺🇸 United States

REUNION

DI: 07613327354331 · Model: 5542-K-0056-A · Stryker Trauma SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REUNION
Primary DI
07613327354331
Version / Model
5542-K-0056-A
Catalog Number
5542-K-0056-A
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-15
Public Version
2
Public Version Date
2023-08-11
Public Version Status
Update
Public Device Record Key
987befc1-a503-46bd-863c-9481b9d9044d
Distribution End Date
2022-11-15

Device Description

X3 KEELED GLENOID

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
35670 Total shoulder prosthesis

Identifiers

Type ID
Primary 07613327354331