FDA UDI In Commercial Distribution 🇺🇸 United States

REDAPT

DI: 00885556321942 · Model: 71354245 · Smith & Nephew, Inc.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REDAPT
Primary DI
00885556321942
Version / Model
71354245
Catalog Number
71354245
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-24
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
e1fc6d8f-cced-4c88-bc40-d77df77002d2

Device Description

REDAPT FULLY POROUS SHELL 78MM

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer

GMDN Terms

Code Name
43167 Acetabular shell

Identifiers

Type ID
Primary 00885556321942

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150790 000
K211176 000