FDA UDI In Commercial Distribution 🇺🇸 United States

REDAPT

DI: 00885556486597 · Model: 71355121 · Smith & Nephew, Inc.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REDAPT
Primary DI
00885556486597
Version / Model
71355121
Catalog Number
71355121
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-15
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
c9e4767e-7b23-45e8-bf5e-2351c33222fd

Device Description

REDAPT REVISION ACETABULAR DRILL GUIDE

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
No
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
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00885556486597

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150790 000