FDA UDI In Commercial Distribution 🇺🇸 United States

Titan Humeral Resurfacing Arthroplasty

DI: 00885556837306 · Model: SHP-900-40/16 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titan Humeral Resurfacing Arthroplasty
Primary DI
00885556837306
Version / Model
SHP-900-40/16
Catalog Number
SHP-900-40/16
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-22
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a001b415-36d1-4d79-aecf-8a28b0a08851

Device Description

HRA SHAPER SZ. 40/16

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
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

GMDN Terms

Code Name
10455 Bone cutter

Identifiers

Type ID
Primary 00885556837306

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142413 000