FDA UDI In Commercial Distribution 🇺🇸 United States

SYNERGY

DI: 03596010429650 · Model: 71366712 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SYNERGY
Primary DI
03596010429650
Version / Model
71366712
Catalog Number
71366712
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
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
46ccf0b6-a7d6-4a64-ac4e-c6a83a36d9e4

Device Description

SYNERGY FULLY TOOTHED BROACH SIZE 12

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
JDG Prosthesis, hip, femoral component, cemented, metal

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 03596010429650

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123598 000