FDA UDI In Commercial Distribution 🇺🇸 United States

CHARLOTTE

DI: 00840420190420 · Model: 41112002 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CHARLOTTE
Primary DI
00840420190420
Version / Model
41112002
Catalog Number
41112002
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
6
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
609e8029-ec7c-4b96-8dfa-86278e1bffd2

Device Description

MTP Fusion Cup Reamer

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

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00840420190420

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: 16mm