FDA UDI In Commercial Distribution 🇺🇸 United States

Made-To-Order

DI: 00889797109017 · Model: SMS00603 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Made-To-Order
Primary DI
00889797109017
Version / Model
SMS00603
Catalog Number
SMS00603
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
76020561-dfcc-40bb-95a3-c75cb93f2f28

Device Description

Fusion Reaming Core Saw

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
Yes
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
No
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
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00889797109017

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 6 Millimeter