FDA UDI In Commercial Distribution 🇺🇸 United States

PROSTEP

DI: 00889797071970 · Model: 57S1MI08 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROSTEP
Primary DI
00889797071970
Version / Model
57S1MI08
Catalog Number
57S1MI08
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-23
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
06a770b5-e8cb-436c-8f86-3e909b82598d

Device Description

MIS Sterile Instrument Pack w/ Blade & Burr

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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
61688 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00889797071970

Customer Contacts