FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC™ 2 LapiFuse™

DI: 00889797076692 · Model: 38140002 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOLOC™ 2 LapiFuse™
Primary DI
00889797076692
Version / Model
38140002
Catalog Number
38140002
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-12
Public Version
1
Public Version Date
2022-08-22
Public Version Status
New
Public Device Record Key
23b0c566-19f6-4376-85f0-e4d143b2dea0

Device Description

Lapidus Hintermann Distractor

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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GAD RETRACTOR

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00889797076692

Customer Contacts