FDA UDI Not in Commercial Distribution 🇺🇸 United States

REDUX

DI: 00885556539163 · Model: 14770 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REDUX
Primary DI
00885556539163
Version / Model
14770
Catalog Number
14770
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-28
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0493afe0-848a-463a-846e-cd6b6e78ea98
Distribution End Date
2022-03-17

Device Description

WAVE WASHER

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
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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00885556539163

Customer Contacts