FDA UDI In Commercial Distribution 🇺🇸 United States

PROSTEP MICA

DI: 00889797072809 · Model: 57S1L122 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROSTEP MICA
Primary DI
00889797072809
Version / Model
57S1L122
Catalog Number
57S1L122
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-18
Public Version
1
Public Version Date
2022-08-26
Public Version Status
New
Public Device Record Key
25c4c1e8-407e-4c1f-b29a-ede4c89cfcff

Device Description

Drill Bit

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

GMDN Terms

Code Name
43390 Fluted surgical drill bit, single-use

Identifiers

Type ID
Primary 00889797072809

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 2.2 Millimeter
Device Size Text, specify Solid
Device Size Text, specify Long