FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC 3Di CROSSCHECK

DI: 00840420187826 · Model: 582SX3522 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ORTHOLOC 3Di CROSSCHECK
Primary DI
00840420187826
Version / Model
582SX3522
Catalog Number
582SX3522
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
5d74a5c4-4164-4320-9522-8ce4bc70af16

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
HRS Plate, fixation, bone

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00840420187826

Customer Contacts

Device Sizes

Type Value Unit Text
Length 22 Millimeter
Device Size Text, specify Thread Length: 15mm
Outer Diameter 3.5 Millimeter