FDA UDI In Commercial Distribution 🇺🇸 United States

Titan Reverse Shoulder System

DI: 00885556863916 · Model: IMP-0960-064-01 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titan Reverse Shoulder System
Primary DI
00885556863916
Version / Model
IMP-0960-064-01
Catalog Number
IMP-0960-064-01
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-02
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
160d2b74-6685-4612-9297-33182b36def2

Device Description

GLENOID BASEPLATE IMPACTOR MOD

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
HWA IMPACTOR

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 00885556863916

Customer Contacts