FDA UDI In Commercial Distribution 🇺🇸 United States

SPECTRON

DI: 03596010195579 · Model: 71312112 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SPECTRON
Primary DI
03596010195579
Version / Model
71312112
Catalog Number
71312112
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-04
Public Version
7
Public Version Date
2025-11-13
Public Version Status
Update
Public Device Record Key
272c77db-5441-423b-8c4c-18dfb71ade43

Device Description

SPECTRON EF PRIMARY HIGH OFFSET 12/14 FEMORAL SIZE 2

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
MR Conditional
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
MRA Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented

GMDN Terms

Code Name
34190 Uncoated hip femur prosthesis, modular

Identifiers

Type ID
Primary 03596010195579

Customer Contacts