FDA UDI In Commercial Distribution 🇺🇸 United States

EVOLVE

DI: 00840420191595 · Model: 24991055 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EVOLVE
Primary DI
00840420191595
Version / Model
24991055
Catalog Number
24991055
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
4
Public Version Date
2022-08-11
Public Version Status
Update
Public Device Record Key
da5f9c84-ad44-4aba-b66c-68ecbaca47ca

Device Description

Proline Stem Paddle

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
59009 Orthopaedic implant/instrument assembling device

Identifiers

Type ID
Primary 00840420191595

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: 5.5mm