FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC 3DI

DI: 00889797101110 · Model: 58A10001 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOLOC 3DI
Primary DI
00889797101110
Version / Model
58A10001
Catalog Number
58A10001
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-10
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
9e94c095-62ce-43fd-9803-636704605afa

Device Description

Fusion Plate

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
Yes
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HRS Plate, fixation, bone

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00889797101110

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Step: 1mm