FDA UDI In Commercial Distribution 🇺🇸 United States

TANDEM

DI: 03596010498137 · Model: 71322038 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TANDEM
Primary DI
03596010498137
Version / Model
71322038
Catalog Number
71322038
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a989565d-ca2c-4bc9-87dd-04b747085876

Device Description

TANDEM BIPOLAR COBALT CHROME 38MM OUTER DIAMETER 22MM INNER DIAMETER

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
33695 Bipolar femoral head outer component, hemiarthroplasty

Identifiers

Type ID
Primary 03596010498137

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K023743 000