FDA UDI In Commercial Distribution 🇺🇸 United States

REDAPT

DI: 00885556587614 · Model: 71355375 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REDAPT
Primary DI
00885556587614
Version / Model
71355375
Catalog Number
71355375
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-23
Public Version
10
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
593771ac-3ae5-4d95-b3fd-e5a0a0b746bd

Device Description

REDAPT REVISION ACETABULAR STAPLE AUGMENT TRIAL TRAY

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00885556587614

Customer Contacts