FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC 3Di

DI: 00889797101257 · Model: 58A92020 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOLOC 3Di
Primary DI
00889797101257
Version / Model
58A92020
Catalog Number
58A92020
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-29
Public Version
3
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
d93459fd-8f0f-4792-8ca6-a76c87c3acea

Device Description

Plating

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
61807 Bone-resection orthopaedic reamer, single-use

Identifiers

Type ID
Primary 00889797101257

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: 20mm
Device Size Text, specify Size 20 mm