FDA UDI In Commercial Distribution 🇺🇸 United States

Corin BiPolar-i

DI: 05056139234064 · Model: 2110059 · CORIN LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Corin BiPolar-i
Primary DI
05056139234064
Version / Model
2110059
Catalog Number
2110059
Company Name
CORIN LTD
Labeler DUNS
295437313
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-25
Public Version
1
Public Version Date
2019-08-02
Public Version Status
New
Public Device Record Key
1f1fa3e7-6c0e-45b3-89fc-a621753ea945

Device Description

Acetabular Trial Ø59

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

GMDN Terms

Code Name
58479 Femoral head prosthesis trial

Identifiers

Type ID
Primary 05056139234064

Premarket Submissions

Submission Number Supplement Number
K183114 000