FDA UDI In Commercial Distribution 🇺🇸 United States

REUNION

DI: 07613327424973 · Model: 5567-P-3013 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REUNION
Primary DI
07613327424973
Version / Model
5567-P-3013
Catalog Number
5567-P-3013
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-05
Public Version
1
Public Version Date
2019-03-13
Public Version Status
New
Public Device Record Key
84c4c6bf-e79d-48bf-9a26-79c880b88999

Device Description

Press-fit Humeral Stem

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
MR Conditional
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
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
35670 Total shoulder prosthesis

Identifiers

Type ID
Primary 07613327424973

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 13.0 Millimeter
Length 97.0 Millimeter